FDA UDI In Commercial Distribution 🇺🇸 United States

COVERIS

DI: B030CS1061320 · Model: CS-106-132 · CAMBER SPINE TECHNOLOGIES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
COVERIS
Primary DI
B030CS1061320
Version / Model
CS-106-132
Company Name
CAMBER SPINE TECHNOLOGIES, LLC
Labeler DUNS
054205979
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-27
Public Version
1
Public Version Date
2023-11-06
Public Version Status
New
Public Device Record Key
e16c9338-5fab-4b89-a0e6-40bdf2bb9bff

Device Description

Rasp, 12.5mm x 16mm, Parallel, 7mm

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
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
HTR Rasp

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary B030CS1061320

Customer Contacts