FDA UDI In Commercial Distribution 🇺🇸 United States

ATEC A.R.M.

DI: 00190376678832 · Model: 202-900 · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ATEC A.R.M.
Primary DI
00190376678832
Version / Model
202-900
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-23
Public Version
1
Public Version Date
2025-12-31
Public Version Status
New
Public Device Record Key
28fc5095-a3a8-4ed9-a515-b69fcd365316

Device Description

Pneumatic Actuation and Regulation System 2.0

Device Characteristics

Single Use
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FQO Table, operating-room, ac-powered
FWW Table, operating-room, pneumatic

GMDN Terms

Code Name
67435 Operating table orthopaedic extension, electrically-powered

Identifiers

Type ID
Primary 00190376678832

Customer Contacts