FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982198051 · Model: 390.037 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982198051
Version / Model
390.037
Catalog Number
390037
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
6
Public Version Date
2023-02-22
Public Version Status
Update
Public Device Record Key
56b4acb3-6bd1-4bd9-9977-ed59b9a102a7

Device Description

8.0MM/11.0MM COMBINATION 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
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
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 H6793900370
Primary 10886982198051
Direct Marking 07611819784215

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040258 000
K090658 000
K161417 000