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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
Bone file/rasp, manual, reusable FDA UDI
Device Name
Peet Diamond Rasp, curved FDA UDI
Model / Reference
56-5153 FDA UDI
Description
Peet Diamond Rasp, curved FDA UDI

Identifiers

Catalog Number
56-5153 FDA UDI
Primary DI / UDI-DI
B7685651530 FDA UDI
FDA Product Code
GAC FDA UDI
GMDN Term
Bone file/rasp, manual, reusable 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: Bone file/rasp, manual, reusable

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

Similar devices

Also classified as Bone file/rasp, manual, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 63d693d4-2112-4ef6-aa30-fb02e9295638 34 fields · synced Jun 1, 2026