FDA UDI In Commercial Distribution 🇺🇸 United States

ATB

DI: 10705034712062 · Model: 03.601.172 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ATB
Primary DI
10705034712062
Version / Model
03.601.172
Catalog Number
03601172
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
2019-02-07
Public Version Status
Update
Public Device Record Key
34bc6e52-b3f7-4660-b388-d0838f2b4e9a

Device Description

ANTERIOR TENSION BAND TEMPLATE TWO LEVEL SYMMETRICAL 81MM

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
HWT TEMPLATE

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Secondary H981036011720
Primary 10705034712062

Customer Contacts