FDA UDI In Commercial Distribution 🇺🇸 United States

TWINFIX

DI: 03596010579386 · Model: 72200780 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TWINFIX
Primary DI
03596010579386
Version / Model
72200780
Catalog Number
72200780
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-21
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
7527d6c7-06c7-49da-8fa5-5af541cc145b

Device Description

6.5 MM TWINFIX AB SUTURE ANCHOR, PLLA, WITH TWO No.2 PRELOADED ULTRABRAID SUTURES, PACKAGED WITH THREADED DILATOR, STERILE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
MAI FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE

GMDN Terms

Code Name
45061 Tendon/ligament bone anchor, bioabsorbable

Identifiers

Type ID
Primary 03596010579386

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K151105 000