Section A: certification type and date
Initial, revised or recertification dates. The instructions say a revised or recertified CMN always gives the initial date as well.
CMS-847
Certificate of Medical Necessity - Osteogenesis Stimulators - DME 04.04C
Form CMS-847 is the Certificate of Medical Necessity (CMN) for osteogenesis stimulators from the Centers for Medicare & Medicaid Services (CMS), part of the U.S. Department of Health and Human Services. The form is printed as DME 04.04C. Its instructions say the question section gathers clinical information to help Medicare determine the medical necessity for the items being ordered, and the CMS page notes the form is to be used starting January 1, 2007.
The form has four sections. Section A identifies the patient, supplier, place of service, procedure codes, facility and physician, and may be completed by the supplier. Section B covers the estimated length of need, diagnosis codes and questions on nonspinal electrical, spinal electrical and ultrasonic osteogenesis stimulators, and may not be completed by the supplier. Section C describes the equipment and its cost, and Section D is the physician's attestation and signature.
The form says signature and date stamps are not acceptable. You can fill it out free in your browser on this page and download the result without an account.

Initial, revised or recertification dates. The instructions say a revised or recertified CMN always gives the initial date as well.
Patient and supplier details with NSC or NPI number, place of service, facility, procedure codes, date of birth, sex, height and weight, and the physician's name, address, phone and UPIN or NPI.
Estimated length of need in months, 1 to 99, where 99 means lifetime, and diagnosis codes, up to 4.
Questions 1 to 5 are blank. Questions 6 to 8 are for a nonspinal electrical stimulator and ask about fracture healing, failed fusion of a joint other than the spine and congenital pseudoarthrosis. Questions 6 and 12 are for an ultrasonic stimulator.
For a spinal electrical stimulator: a failed single level spinal fusion, an adjunct to repeat single level fusion, and multi-level spinal fusion, with months since each fusion where asked.
Section C: a narrative description of all items, accessories and options ordered, the supplier's charge and the Medicare fee schedule allowance for each. Section D: the physician's attestation, signature and date.
Enter the certification type and date, patient, supplier, place of service, procedure codes and physician details. The instructions say procedure codes that do not require certification should not be listed.
The instructions say to use XX before a 10-digit NPI, 1C before a legacy NSC number and 1G before a 6-digit UPIN.
Enter the length of need and diagnosis codes, then answer the questions for the stimulator type ordered with Y, N or D. For month questions the form says to enter 1 to 99 or D, and 1 if less than one month.
If someone other than the treating physician answered Section B, they print their name, professional title and employer. If the physician answered, the instructions say the space may be left blank.
Describe each item, option, accessory, supply and drug ordered, with the supplier's charge and the Medicare fee schedule allowance for each, if applicable.
After completing or reviewing Sections A, B and C, the physician signs and dates Section D. The form says signature and date stamps are not acceptable.
You get the real form, filled in a browser tab, with nothing standing between you and the finished PDF.
The form does not print a submission address. The CMS address in the Paperwork Reduction Act notice is for comments on the form, and the form says not to submit claims to it. It points to medicare.gov for information on claim filing.
The instructions say a revised certification is completed when the physician changes the order based on the patient's changing clinical needs, and that the initial date is always given along with the revised or recertification date.
The instructions give examples: patient's home is 12, skilled nursing facility (SNF) is 31 and End Stage Renal Disease (ESRD) facility is 65. They refer to the DMERC supplier manual for a complete list.
Section D says any falsification, omission or concealment of material fact in Section B may subject the physician to civil or criminal liability.
The form estimates an average of 12 minutes per response, including reviewing the instructions and gathering the data. It shows OMB No. 0938-0679.
CMS-484
95 fields, 2 pages
CMS-849
32 fields, 2 pages
CMS-10126
96 fields, 2 pages
CMS-10269
89 fields, 2 pages
CMS-855S
1,031 fields, 39 pages
The instructions say Section A may be completed by the supplier, and Section C, the narrative description of equipment and cost, is completed by the supplier.
Section D is completed by the physician, whose signature certifies the CMN, the answers in Section B and the information in Section A.
The instructions say a non-physician clinician or a physician employee may complete Section B and print their name, title and employer. The treating practitioner still reviews it and signs the CMN.
Section A records the patient's name, permanent legal address, telephone number and Medicare ID as it appears on the Medicare card and on the claim form.
The form splits its sections between the supplier and the physician.
The agency’s own page for Form CMS-847.
The official blank form, to print or fill by hand.
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The supplier may complete Section A and completes Section C. Section B may not be completed by the supplier. The treating physician completes Section D and signs the form.
No. The form says information in Section B may not be completed by the supplier of the items or supplies. A non-physician clinician or physician employee may complete it, but the treating practitioner reviews it and signs the CMN.
The form says questions 1 to 5 are blank. Questions 6 to 8 are for a nonspinal electrical osteogenesis stimulator, questions 9 to 11 for a spinal electrical stimulator, and questions 6 and 12 for an ultrasonic stimulator.
The form uses 99 for lifetime. The instructions say to enter 99 if the patient will require the item for the duration of their life, and otherwise the number of months.
No. The form says signature and date stamps are not acceptable.
No. The form says do not submit claims to the CMS address in its Paperwork Reduction Act notice, and points to medicare.gov for information on claim filing.