FDA UDI Not in Commercial Distribution 🇺🇸 United States

CANYON Retractor Systems

DI: 10888857443501 · Model: AN01-91112 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CANYON Retractor Systems
Primary DI
10888857443501
Version / Model
AN01-91112
Catalog Number
AN01-91112
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-23
Public Version
2
Public Version Date
2023-09-08
Public Version Status
Update
Public Device Record Key
39aa3e32-4080-455f-a563-44036a4aa7d4
Distribution End Date
2023-09-07

Device Description

Slotted Port Size Ø12x120 mm

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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 10888857443501

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 12 Millimeter
Length 120 Millimeter