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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-extraction orthopaedic reamer, reusable FDA UDI
Device Name
BIT, INT.SCREW REMOVER 4.0MM 1/4 SQ FDA UDI
Model / Reference
925-0901 FDA UDI
Description
BIT, INT.SCREW REMOVER 4.0MM 1/4 SQ FDA UDI

Identifiers

Catalog Number
925-0901 FDA UDI
Primary DI / UDI-DI
00810019931284 FDA UDI
FDA Product Code
HXX FDA UDI
GMDN Term
Screw-extraction orthopaedic reamer, 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-extraction orthopaedic reamer, 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-extraction orthopaedic reamer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bradshaw Medical Inc.

Sources (1)

  • FDA UDI 87994e4a-c921-414f-8945-dbd64be6cde0 35 fields · synced May 30, 2026