FDA UDI In Commercial Distribution 🇺🇸 United States

CANNU-FLEX SILK

DI: 03596010025579 · Model: 014200 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CANNU-FLEX SILK
Primary DI
03596010025579
Version / Model
014200
Catalog Number
014200
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
7
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
40f16dee-a207-4594-b354-3a0d8baed790

Device Description

CANNU-FLEX 7 MM X 20 MM 1.0 SCREW, STERILE

Device Characteristics

Single Use
Yes
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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, fixation, bone

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 03596010025579

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K921481 000