FDA UDI In Commercial Distribution 🇺🇸 United States

Sigma

DI: 00811801038822 · Model: CI-10531-200-100 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sigma
Primary DI
00811801038822
Version / Model
CI-10531-200-100
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
3b00a5df-858b-42d0-8396-0b362d19fb53

Device Description

Sigma Medial Blade, Non-ratcheting, X-Large

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 00811801038822

Customer Contacts