FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10888551024259 · Model: SYN395.56 · STERILMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10888551024259
Version / Model
SYN395.56
Catalog Number
SYN395.56
Company Name
STERILMED, INC.
Labeler DUNS
175899459
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-22
Public Version
4
Public Version Date
2019-08-14
Public Version Status
Update
Public Device Record Key
b2033a9d-be0c-4f26-9e16-e54b3fb5fe7c

Device Description

SYNTHES CLAMP

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
No
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
46453 External orthopaedic fixation system reprocessed component

Identifiers

Type ID
Primary 10888551024259

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K051957 000