FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982290243 · Model: 04.233.121S · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982290243
Version / Model
04.233.121S
Catalog Number
04233121S
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-21
Public Version
4
Public Version Date
2023-06-16
Public Version Status
Update
Public Device Record Key
5587834b-2b99-4275-a06c-9545cfb9ba96

Device Description

RFNA / 11MM / 200MM PERIPROSTHETIC BEND / STERILE

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, fixation, bone
HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

GMDN Terms

Code Name
33187 Femur nail

Identifiers

Type ID
Primary 10886982290243

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201346 000