FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10888551024402 · Model: SYN395.786 · STERILMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10888551024402
Version / Model
SYN395.786
Catalog Number
SYN395.786
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
03ec4858-2cd9-4884-8c4c-b3f00331e338

Device Description

SYNTHES ROD CARBON FIBER

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 10888551024402

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K051957 000