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Guide Pin/Screw

FDA UDI

Class II (US FDA UDI)

by Gebr. Brasseler GmbH & Co. KG

Identity

Trade Name
GUIDE PIN/SCREW FDA UDI
Generic Name
Orthopaedic intraoperative positioning pin, single-use FDA UDI
Model / Reference
OC907A.076.032 STE FDA UDI

Identifiers

Catalog Number
OC907A.076.032 STE FDA UDI
Primary DI / UDI-DI
14053613278970 FDA UDI
510(k) Number
K131264 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic intraoperative positioning pin, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic intraoperative positioning pin, single-use

Guide Pin/Screw by Gebr. Brasseler GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic intraoperative positioning pin, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5caa2bcf-2e0f-4c54-a97b-20fcf008d319 34 fields · synced May 30, 2026