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Bradshaw Medical Inc.

FDA UDI

Class I (US FDA UDI)

by Bradshaw Medical Inc.

Identity

Trade Name
Bradshaw Medical Inc. FDA UDI
Generic Name
Screw extractor, reusable FDA UDI
Device Name
BIT, EXT. SCREW REMOVER 3.0MM 1/4 SQ FDA UDI
Model / Reference
925-1002 FDA UDI
Description
BIT, EXT. SCREW REMOVER 3.0MM 1/4 SQ FDA UDI

Identifiers

Catalog Number
925-1002 FDA UDI
Primary DI / UDI-DI
00810019931345 FDA UDI
FDA Product Code
HXX FDA UDI
GMDN Term
Screw extractor, 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Screw extractor, reusable

Bradshaw Medical Inc. by Bradshaw Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screw extractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b8fde0a2-7996-4f8a-93d2-ad189fe152f3 35 fields · synced May 30, 2026