FDA UDI In Commercial Distribution 🇺🇸 United States

Intervertebral Disc Preparation Instruments

DI: 00190376380971 · Model: 256-15-100-1604 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Intervertebral Disc Preparation Instruments
Primary DI
00190376380971
Version / Model
256-15-100-1604
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-18
Public Version
1
Public Version Date
2021-12-27
Public Version Status
New
Public Device Record Key
2b0b6abc-3084-41e0-9415-711408005cb0

Device Description

LIF, BROACH, CC OFFSET, 16MM X 04MM

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
HTQ BROACH

GMDN Terms

Code Name
10455 Bone cutter

Identifiers

Type ID
Primary 00190376380971

Customer Contacts

Device Sizes

Type Value Unit Text
Height 4 Millimeter
Width 16 Millimeter