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Gpc

FDA UDI

Class I (US FDA UDI)

by Gpc Medical, Ltd.

Identity

Trade Name
GPC FDA UDI
Generic Name
General internal orthopaedic fixation system implantation kit FDA UDI
Device Name
4.5mm Herbert Screw Instrument Set Star Drive FDA UDI
Model / Reference
S-HS-SD1434.45 FDA UDI
Description
4.5mm Herbert Screw Instrument Set Star Drive FDA UDI

Identifiers

Primary DI / UDI-DI
08904400224139 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
General internal orthopaedic fixation system implantation kit 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

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

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: General internal orthopaedic fixation system implantation kit

Gpc by Gpc Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General internal orthopaedic fixation system implantation kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gpc Medical, Ltd.

Sources (1)

  • FDA UDI 054d6b0a-10cf-4cb0-bda7-5203291115d9 34 fields · synced May 30, 2026