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Zimmer

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
ZIMMER FDA UDI
Generic Name
Surgical drill chuck FDA UDI
Device Name
ZIMMER DRILL (HUDSON MODIFIED TRINKLE) FDA UDI
Model / Reference
72204102 FDA UDI
Description
ZIMMER DRILL (HUDSON MODIFIED TRINKLE) FDA UDI

Identifiers

Catalog Number
72204102 FDA UDI
Primary DI / UDI-DI
00885554033335 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Surgical drill chuck 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical drill chuck

Zimmer by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill chuck.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI e798c88f-df47-42ed-8abf-0b5927118494 35 fields · synced Jun 8, 2026