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Dermatome

FDA UDI

Class I (US FDA UDI)

by Zimmer Orthopaedic Surgical Products

Identity

Trade Name
Dermatome FDA UDI
Generic Name
Dermatome handpiece, electrically-powered FDA UDI
Device Name
Dermatome 2" Width Plate FDA UDI
Model / Reference
00-8802-002-00 FDA UDI
Description
Dermatome 2" Width Plate FDA UDI

Identifiers

Catalog Number
00-8802-002-00 FDA UDI
Primary DI / UDI-DI
00889024375949 FDA UDI
FDA Product Code
GFD FDA UDI
GMDN Term
Dermatome handpiece, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 2 Inch FDA UDI

Category: Dermatome handpiece, electrically-powered

Dermatome by Zimmer Orthopaedic Surgical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatome handpiece, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer Orthopaedic Surgical Products

Sources (1)

  • FDA UDI 31f3ce72-d29c-46de-834d-a8c7061f3dff 36 fields · synced May 30, 2026