FDA UDI In Commercial Distribution 🇺🇸 United States

LCP

DI: 10886982074010 · Model: 03.120.003 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
LCP
Primary DI
10886982074010
Version / Model
03.120.003
Catalog Number
03120003
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
4
Public Version Date
2022-04-28
Public Version Status
Update
Public Device Record Key
333ab0a2-c006-48cb-b57b-23047f356b7e

Device Description

OBLQUE AIM GUIDE F/PERIART ARM F/4.5MM LCP PROX TIBIA PL-RT

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FZX Guide, surgical, instrument

GMDN Terms

Code Name
47786 Orthopaedic implant aiming arm

Identifiers

Type ID
Direct Marking 07611819969964
Secondary H679031200030
Primary 10886982074010

Customer Contacts