FDA UDI In Commercial Distribution 🇺🇸 United States

Prolix

DI: B030CW1300050 · Model: CW-130-005 · CAMBER SPINE TECHNOLOGIES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Prolix
Primary DI
B030CW1300050
Version / Model
CW-130-005
Company Name
CAMBER SPINE TECHNOLOGIES, LLC
Labeler DUNS
054205979
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-03
Public Version
1
Public Version Date
2023-11-13
Public Version Status
New
Public Device Record Key
edaa9011-de16-47ef-92f1-bd06d78f199b

Device Description

Ø2mm x 190mm Steinmann Pin, Round Tip

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
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
47900 Orthopaedic implant calibration pin

Identifiers

Type ID
Primary B030CW1300050

Customer Contacts