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Buxton BioMedical

FDA UDI

Class I (US FDA UDI)

by Buxton Biomedical, Inc.

Identity

Trade Name
Buxton BioMedical FDA UDI
Generic Name
Orthopaedic chisel blade FDA UDI
Device Name
Chisel Blade, 16mm wide FDA UDI
Model / Reference
24-4216 FDA UDI
Description
Chisel Blade, 16mm wide FDA UDI

Identifiers

Catalog Number
24-4216 FDA UDI
Primary DI / UDI-DI
B7682442160 FDA UDI
FDA Product Code
HWM FDA UDI
GMDN Term
Orthopaedic chisel blade FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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: Orthopaedic chisel blade

Buxton BioMedical by Buxton Biomedical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic chisel blade.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f0c15173-1dc2-4af8-b267-9f48f89cdceb 34 fields · synced May 31, 2026