FDA UDI Not in Commercial Distribution 🇺🇸 United States

SynFix-LR

DI: 10705034722252 · Model: 03.802.039 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SynFix-LR
Primary DI
10705034722252
Version / Model
03.802.039
Catalog Number
03802039
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
7
Public Version Date
2021-04-21
Public Version Status
Update
Public Device Record Key
68f7cf62-e474-4b09-b107-79daf56760d0
Distribution End Date
2020-09-17

Device Description

IMPLANT HOLDER FOR SYNFIX(TM)-LR

Device Characteristics

Single Use
No
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
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Direct Marking 07611819297234
Secondary H981038020390
Primary 10705034722252

Customer Contacts