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Lcs Completion

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 2178-63-135Model LPS Assembly Instrument

by Depuy Orthopaedics, Inc.

Identity

Trade Name
LCS COMPLETION EUDAMEDFDA UDI
Generic Name
Orthopaedic implant/instrument assembling device FDA UDI
Device Name
Assembly Instrument EUDAMED
LCS Completion REV FEM STEM/ADAPT CLAMP 13mm FDA UDI
Model / Reference
2178-63-135 EUDAMEDFDA UDI
LPS Assembly Instrument EUDAMED
Description
LCS Completion REV FEM STEM/ADAPT CLAMP 13mm FDA UDI

Identifiers

Catalog Number
217863135 FDA UDI
Primary DI / UDI-DI
10603295096245 EUDAMEDFDA UDI
Basic UDI-DI
0603295a000307X EUDAMED
Direct Marketing DI
10603295096245 EUDAMED
FDA Product Code
HXD FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic implant/instrument assembling device FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

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: Orthopaedic implant/instrument assembling device

Lcs Completion by Depuy Orthopaedics, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant/instrument assembling device.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 91ecc0ca-ec3c-4b5b-b378-cefa0049de96 35 fields · synced Jun 19, 2026
  • EUDAMED 521c1069-fcbf-42e0-92a6-cc93a14138d9 61 fields · synced Jun 19, 2026