FDA UDI In Commercial Distribution 🇺🇸 United States

SynCage

DI: 10705034778488 · Model: 397.081 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SynCage
Primary DI
10705034778488
Version / Model
397.081
Catalog Number
397081
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
d7cee627-ca19-4bf8-b6a9-59dcdd01863a

Device Description

SYNCAGE ANTERIOR DISTRACTOR

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
HWB EXTRACTOR

GMDN Terms

Code Name
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Direct Marking 07611819220799
Secondary H9813970810
Primary 10705034778488

Customer Contacts