FDA UDI In Commercial Distribution 🇺🇸 United States

SynFix-LR

DI: 10705034778570 · Model: 397.113 · 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
10705034778570
Version / Model
397.113
Catalog Number
397113
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
2016-12-31
Public Version
3
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
ff545de7-5ea3-4b99-8981-1ad1b2ef025a

Device Description

DISTRACTOR 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
HTD FORCEPS

GMDN Terms

Code Name
44378 Bone distraction forceps

Identifiers

Type ID
Direct Marking 07611819254688
Secondary H9813971130
Primary 10705034778570

Customer Contacts