← Back to catalogue

V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Bone holding forceps FDA UDI
Device Name
V. Mueller LOCKE PHALANGEAL FORCEPS 1 X 2 TEETH SERRATED OVERALL LENGTH 6 inches 15.2CM FDA UDI
Model / Reference
OS4805 FDA UDI
Description
V. Mueller LOCKE PHALANGEAL FORCEPS 1 X 2 TEETH SERRATED OVERALL LENGTH 6 inches 15.2CM FDA UDI

Identifiers

Catalog Number
OS4805 FDA UDI
Primary DI / UDI-DI
10885403105043 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone holding forceps 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: Bone holding forceps

V. Mueller by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone holding forceps.

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

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 0bf0679c-083a-41ec-903f-7649ed5ac87b 35 fields · synced Jun 8, 2026