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Fps

FDA UDI

Class I (US FDA UDI)

by Tyber Medical

Identity

Trade Name
FPS FDA UDI
Generic Name
Orthopaedic fixation plate bending insert, reusable FDA UDI
Device Name
Ø3.0/3.5/4.0mm Bending Pin FDA UDI
Model / Reference
F25-003030 FDA UDI
Description
Ø3.0/3.5/4.0mm Bending Pin FDA UDI

Identifiers

Catalog Number
F25-003030 FDA UDI
Primary DI / UDI-DI
00810040688485 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic fixation plate bending insert, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic fixation plate bending insert, reusable

Fps by Tyber Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate bending insert, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tyber Medical

Sources (1)

  • FDA UDI df06e7ad-2666-4f37-a91f-d9fe61855e9f 35 fields · synced May 30, 2026