FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982274281 · Model: 04.168.080S · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982274281
Version / Model
04.168.080S
Catalog Number
04168080S
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-25
Public Version
4
Public Version Date
2024-02-27
Public Version Status
Update
Public Device Record Key
9c7a193e-9387-4809-a399-7a9c8c3c6447

Device Description

FEMORAL NECK SYSTEM IMPLANT KIT/ LENGTH 80MM STERILE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 10886982274281

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K172872 000