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Zimmer Biomet™

FDA UDI

Class I (US FDA UDI)

by Zimmer Surgical SA

Identity

Trade Name
Zimmer Biomet™ FDA UDI
Generic Name
Surgical power tool battery-exchange sterility cover FDA UDI
Model / Reference
89-8521-470-40 FDA UDI

Identifiers

Catalog Number
89-8521-470-40 FDA UDI
Primary DI / UDI-DI
00889024581746 FDA UDI
FDA Product Code
MOQ FDA UDI
GMDN Term
Surgical power tool battery-exchange sterility cover 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical power tool battery-exchange sterility cover

Zimmer Biomet™ by Zimmer Surgical SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool battery-exchange sterility cover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer Surgical SA

Sources (1)

  • FDA UDI d3b05f52-8c99-4bf0-ac9f-bd3426e86228 34 fields · synced May 30, 2026