FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982079541 · Model: 03.390.052S · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982079541
Version / Model
03.390.052S
Catalog Number
03390052S
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
7
Public Version Date
2024-02-27
Public Version Status
Update
Public Device Record Key
0eecfa65-3f9c-492f-89eb-cb06edbdb606

Device Description

DISTAL RADIUS FIXATOR KIT 200MM ROD/SCHANZ SCREW-STERILE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Secondary H67903390052S0
Primary 10886982079541

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K031973 000
K090658 000