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 BONE REDUCTION FORCEPS SPEED LOCK SMALL SERRATED JAW OVERALL LENGTH 7 inches 17.8CM FDA UDI
Model / Reference: OS911-012 FDA UDI
Description: V. Mueller BONE REDUCTION FORCEPS SPEED LOCK SMALL SERRATED JAW OVERALL LENGTH 7 inches 17.8CM FDA UDI

Identifiers

Catalog Number: OS911012 FDA UDI
Primary DI / UDI-DI: 10885403101281 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

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.

Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
gSource — GSOURCE, LLC. · Class I
Thrust Arm, Left, Pelvic Linear Hook Attachment — I.T.S. GmbH · Class I
FORCEPS — KLS-Martin L.P. · Class I
Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
CLAMP — KLS-Martin L.P. · Class I
Novo Surgical — NOVO SURGICAL, INC. · Class I
Tecomet — Tecomet,Inc · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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

Manufacturer

Manufacturer: Steris Corporation

Sources (1)

FDA UDI eebba99b-238a-4780-9144-466f0a2f34e3 35 fields · synced Jun 6, 2026