FDA UDI In Commercial Distribution 🇺🇸 United States

Arsenal

DI: 00840967195995 · Model: 88142-L · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arsenal
Primary DI
00840967195995
Version / Model
88142-L
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-17
Public Version
1
Public Version Date
2020-06-25
Public Version Status
New
Public Device Record Key
9a211fac-c41c-4f93-b969-6a88ae0758cd

Device Description

Fixed Bridge Bender Left

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
HXW BENDER

GMDN Terms

Code Name
44795 Manual orthopaedic bender, reusable

Identifiers

Type ID
Primary 00840967195995

Customer Contacts