FDA UDI Not in Commercial Distribution 🇺🇸 United States

Xenon

DI: 00840967190228 · Model: 22TRV12US · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Xenon
Primary DI
00840967190228
Version / Model
22TRV12US
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-17
Public Version
3
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
1f6dddd6-6850-4d0b-bcf3-8be883fe2e74
Distribution End Date
2023-04-06

Device Description

POLYAXIAL SCREW ADJUSTMENT TOOL

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
HWR DRIVER, PROSTHESIS

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00840967190228

Customer Contacts