FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982200792 · Model: 395.792 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982200792
Version / Model
395.792
Catalog Number
395792
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
5
Public Version Date
2022-10-11
Public Version Status
Update
Public Device Record Key
6415e16b-c78b-48c1-872e-1fc3e549ef9b

Device Description

8.0MM CARBON FIBER ROD 320MM

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

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
Secondary H6793957920
Primary 10886982200792
Direct Marking 07611819738980

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K011034 000
K033158 000
K043039 000