FDA UDI In Commercial Distribution 🇺🇸 United States

General Instruments

DI: 00840180501313 · Model: CI-10629-03-20 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
General Instruments
Primary DI
00840180501313
Version / Model
CI-10629-03-20
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-08
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
50af4626-853c-43b8-95e9-368e6a6e7225

Device Description

Medial/Lateral Angled LIF Curette - SIZE 3, RIGHT

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
HTF CURETTE

GMDN Terms

Code Name
47022 Neurosurgical curette, single-use

Identifiers

Type ID
Primary 00840180501313

Customer Contacts