FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982111173 · Model: 04.124.422S · Synthes GmbH
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982111173
Version / Model
04.124.422S
Catalog Number
04124422S
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-21
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
54c86263-576d-491f-9c27-a829f46d31f2

Device Description

4.5MM TI VA-LCP CRVD CONDYLAR PLATE/22H/439MM/RT-STER

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HRS Plate, fixation, bone
HWC Screw, fixation, bone
JDP condylar plate fixation Implant

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Secondary H67904124422S0
Primary 10886982111173

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K110354 000