FDA UDI In Commercial Distribution 🇺🇸 United States

SynFix

DI: 10705034709451 · Model: SD397.064 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SynFix
Primary DI
10705034709451
Version / Model
SD397.064
Catalog Number
SD397064
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
9b05bae9-0d49-46e8-88cb-b1a27f320014

Device Description

SYNFIX-LR TRIAL RASP 8DEG DEPTH 26MM/W 32MM/H 17MM

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
HTR RASP

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Secondary H981SD3970640
Primary 10705034709451

Customer Contacts