FDA UDI In Commercial Distribution 🇺🇸 United States

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DI: 00190376678733 · Model: CLCCXINT · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Calibrate
Primary DI
00190376678733
Version / Model
CLCCXINT
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-30
Public Version
1
Public Version Date
2025-06-09
Public Version Status
New
Public Device Record Key
fb49b69f-c744-45d0-ac11-ce9e9893a6cd

Device Description

Calibrate CCX Instrument System

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00190376678733

Customer Contacts