FDA UDI In Commercial Distribution 🇺🇸 United States

VA-LCP

DI: 10886982073631 · Model: 03.118.102 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VA-LCP
Primary DI
10886982073631
Version / Model
03.118.102
Catalog Number
03118102
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
6
Public Version Date
2023-09-01
Public Version Status
Update
Public Device Record Key
40988e1c-8c88-4bd8-a64d-12d3b9020053

Device Description

GUIDE BLOCK FOR 2.7/3.5MM VA-LCP ANTLAT DSTL TIB 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
No
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
HRS PLATE, FIXATION, BONE
HWC Screw, fixation, bone

GMDN Terms

Code Name
61929 Orthopaedic implant aiming/guiding block attachment tool

Identifiers

Type ID
Secondary H679031181020
Primary 10886982073631
Direct Marking 07611819503434

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K121601 000