FDA UDI In Commercial Distribution 🇺🇸 United States

General Instruments

DI: 00811801035623 · Model: CI-10531-200-060 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
General Instruments
Primary DI
00811801035623
Version / Model
CI-10531-200-060
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-19
Public Version
1
Public Version Date
2020-09-28
Public Version Status
New
Public Device Record Key
33deb845-a1a2-4cd7-b144-dcc50578af9d

Device Description

Sigma Medial Blade, Non-ratcheting, Medium

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
GAD RETRACTOR

GMDN Terms

Code Name
45181 Surgical retraction system, reusable

Identifiers

Type ID
Primary 00811801035623

Customer Contacts