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Buxton BioMedical

FDA UDI

Class II (US FDA UDI)

by Buxton Biomedical, Inc.

Identity

Trade Name
Buxton BioMedical FDA UDI
Generic Name
Self-retaining surgical retractor, reusable FDA UDI
Device Name
WeitlanerRet,105x25mm,2x3 blnt FDA UDI
Model / Reference
52-5782 FDA UDI
Description
WeitlanerRet,105x25mm,2x3 blnt FDA UDI

Identifiers

Catalog Number
52-5782 FDA UDI
Primary DI / UDI-DI
B7685257820 FDA UDI
FDA Product Code
GAG FDA UDI
GMDN Term
Self-retaining surgical retractor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4740 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: Self-retaining surgical retractor, reusable

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

Similar devices

Also classified as Self-retaining surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 67c6c71a-2f4f-4a48-902b-c4326cced1f6 34 fields · synced May 31, 2026