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Compass

FDA UDI

Class II (US FDA UDI)

by Compass International

Identity

Trade Name
Compass FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Allen Wrench w/handle .050 FDA UDI
Model / Reference
AW-.050-10 FDA UDI
Description
Allen Wrench w/handle .050 FDA UDI

Identifiers

Catalog Number
AW-.050-10 FDA UDI
Primary DI / UDI-DI
B169AW050100 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

Category: Surgical screwdriver, reusable

Compass by Compass International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6465d77b-ee75-4063-8b3d-dee3bcb3ad39 34 fields · synced May 30, 2026