← Back to catalogue

Buxton BioMedical

FDA UDI

Class I (US FDA UDI)

by Buxton Biomedical, Inc.

Identity

Trade Name
Buxton BioMedical FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
Webster Needle Holder, c-j FDA UDI
Model / Reference
52-8121 FDA UDI
Description
Webster Needle Holder, c-j FDA UDI

Identifiers

Catalog Number
52-8121 FDA UDI
Primary DI / UDI-DI
B7685281210 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Suturing needle holder, 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

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: Suturing needle holder, reusable

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

Similar devices

Also classified as Suturing needle holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 6e24c0c9-9984-4808-bafe-75e0f26fafe4 34 fields · synced Jun 6, 2026