FDA UDI In Commercial Distribution 🇺🇸 United States

TWINFIX

DI: 03596010532213 · Model: 7210709 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TWINFIX
Primary DI
03596010532213
Version / Model
7210709
Catalog Number
7210709
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
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
0dc6f63c-7e41-4976-807e-5bee538d8190

Device Description

TWINFIX 6.5 MM TITANIUM SUTURE ANCHOR WITH TWO No.2 PRELOADED ULTRABRAID SUTURES ONE ULTRABRAID WHITE SUTURE AND ONE ULTRABRAID COBRAID SUTURE WITH NEEDLES, 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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBI FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE
JDR STAPLE, FIXATION, BONE

GMDN Terms

Code Name
45061 Tendon/ligament bone anchor, bioabsorbable

Identifiers

Type ID
Primary 03596010532213

Customer Contacts