← Back to catalogue

Lawrence Revision Knee Gap Bal Tensioner Lateral Left

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 1896-01R

by Innomed, Inc.

Identity

Trade Name
Lawrence Revision Knee Gap Bal Tensioner Lateral Left EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Orthopaedic graft tensioner, reusable FDA UDI
Device Name
Extractor EUDAMED
Lawrence Revision Knee Gap Balancing Tensioner Lateral Left FDA UDI
Model / Reference
1896-01R EUDAMED
1896-01L FDA UDI
Description
Lawrence Revision Knee Gap Balancing Tensioner Lateral Left FDA UDI

Identifiers

Catalog Number
1896-01L FDA UDI
Primary DI / UDI-DI
00840277122087 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOEXTRACT0188 EUDAMED
Direct Marketing DI
00840277122087 EUDAMED
FDA Product Code
HWB FDA UDI
EMDN Code
L0921 NON-IMPLANTABLE ORTHOPAEDIC DEVICES EXTRACTORS, REUSABLE EUDAMED
GMDN Term
Orthopaedic graft tensioner, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Lawrence Revision Knee Gap Bal Tensioner Lateral Left by Innomed, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Innomed, Inc.
EUDAMED SRN
US-MF-000014761
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED 5e10f0e5-6b8f-43a5-8114-08828b07a5c2 61 fields · synced Jul 22, 2026
  • FDA UDI 47b9d78c-ef9d-413d-b821-c56d87f766ed 34 fields · synced May 30, 2026