FDA UDI In Commercial Distribution 🇺🇸 United States

CANYON™ Retractor Systems

DI: 10888857436237 · Model: 6401-90183 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CANYON™ Retractor Systems
Primary DI
10888857436237
Version / Model
6401-90183
Catalog Number
6401-90183
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-18
Public Version
3
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
83fb4e0a-6e67-4a2e-bd2a-6e30230d5a04

Device Description

Straight Blade, Size 14x40 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 10888857436237

Customer Contacts

Device Sizes

Type Value Unit Text
Width 14 Millimeter
Length 40 Millimeter