FDA UDI In Commercial Distribution 🇺🇸 United States

VA-LCP

DI: 10886982073129 · Model: 03.115.851 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VA-LCP
Primary DI
10886982073129
Version / Model
03.115.851
Catalog Number
03115851
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
2022-04-28
Public Version Status
Update
Public Device Record Key
3c05d2d1-b028-4b43-9568-8a052568803b

Device Description

SIZING TEMPLATE F/2.4MM VA-LCP VOLAR RIM DSTL RAD PL/7H HD/L

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
HWC Screw, fixation, bone
HRS PLATE, FIXATION, BONE

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Secondary H679031158510
Primary 10886982073129
Direct Marking 07611819453463

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K110125 000