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Zimmer® Natural Nail™ System

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Zimmer® Natural Nail™ System FDA UDI
Generic Name
Hip internal fixation system FDA UDI
Device Name
ZNN CMN LAG SCREW 10.5X130 FDA UDI
Model / Reference
00-2485-130-10 FDA UDI
Description
ZNN CMN LAG SCREW 10.5X130 FDA UDI

Identifiers

Catalog Number
00-2485-130-10 FDA UDI
Primary DI / UDI-DI
00889024276178 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Hip internal fixation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

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: Hip internal fixation system

Zimmer® Natural Nail™ System by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hip internal fixation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 078b1714-9e31-4001-b709-4c94c2c3c027 36 fields · synced May 30, 2026