FDA UDI In Commercial Distribution 🇺🇸 United States

CETRA

DI: 18257200140992 · Model: 450530-0003 · Orthofix US LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CETRA
Primary DI
18257200140992
Version / Model
450530-0003
Catalog Number
19-1111
Company Name
Orthofix US LLC
Labeler DUNS
927083808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-12
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
81911201-7100-4fbc-93b8-37d27150736d

Device Description

CETRA 2.0 - IMPLANT/INSTRUMENT TRAY KIT (19-1111)

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 18257200140992

Customer Contacts