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Walterlorenz™ Surgical Assist Arm

FDA UDI

Class I (US FDA UDI)

by Biomet Microfixation, Inc

Identity

Trade Name
WALTERLORENZ™ SURGICAL ASSIST ARM FDA UDI
Generic Name
Surgical instrument assist arm system structural component FDA UDI
Model / Reference
WAL119 FDA UDI

Identifiers

Catalog Number
WAL119 FDA UDI
Primary DI / UDI-DI
00841036240400 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Surgical instrument assist arm system structural component FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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: Surgical instrument assist arm system structural component

Walterlorenz™ Surgical Assist Arm by Biomet Microfixation, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument assist arm system structural component.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Microfixation, Inc

Sources (1)

  • FDA UDI 186a9bcc-98d2-4ebd-9d76-e228e2d87f0d 34 fields · synced Jun 1, 2026