FDA UDI Not in Commercial Distribution 🇺🇸 United States

CANNU-FLEX

DI: 00885554002690 · Model: 3134108 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CANNU-FLEX
Primary DI
00885554002690
Version / Model
3134108
Catalog Number
3134108
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-12
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
52d728d6-11f4-4d4e-bb0f-9c31af214a09
Distribution End Date
2022-03-17

Device Description

SOD DRIVER SILK SCR 7MM NON-CANNULATED

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
No
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
HRX ARTHROSCOPE

GMDN Terms

Code Name
35138 Meniscus knife

Identifiers

Type ID
Primary 00885554002690

Customer Contacts