FDA UDI In Commercial Distribution 🇺🇸 United States

Trauma Plate System

DI: 00190376484396 · Model: 610-400 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trauma Plate System
Primary DI
00190376484396
Version / Model
610-400
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-05
Public Version
1
Public Version Date
2023-10-13
Public Version Status
New
Public Device Record Key
53d40bac-1fc2-4789-9d21-d068bfa7cb2d

Device Description

Plate Caliper

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
KTZ CALIPER

GMDN Terms

Code Name
35788 Orthopaedic bone calliper

Identifiers

Type ID
Primary 00190376484396

Customer Contacts