FDA UDI In Commercial Distribution 🇺🇸 United States

AMP II

DI: 00190376588575 · Model: 614-201 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
AMP II
Primary DI
00190376588575
Version / Model
614-201
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-20
Public Version
1
Public Version Date
2025-03-28
Public Version Status
New
Public Device Record Key
5a88cc03-a9a4-4594-95e1-ce0c23b55c1a

Device Description

Awl, Offset

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
HWJ AWL

GMDN Terms

Code Name
15275 Bone awl, reusable

Identifiers

Type ID
Primary 00190376588575

Customer Contacts