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Nex-Link®

FDA UDI

Class II (US FDA UDI)

by Zimmer Biomet

Identity

Trade Name
Nex-Link® FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
Transverse Connector - 4 mm Rod - 25 mm FDA UDI
Model / Reference
721-4025 FDA UDI
Description
Transverse Connector - 4 mm Rod - 25 mm FDA UDI

Identifiers

Primary DI / UDI-DI
00887868284687 FDA UDI
FDA Product Code
MNI FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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: Bone-screw internal spinal fixation system, non-sterile

Nex-Link® by Zimmer Biomet — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer Biomet

Sources (1)

  • FDA UDI 3d2bd14e-1631-43ec-bcf1-bd6586c229b5 33 fields · synced Jun 1, 2026