FDA UDI Not in Commercial Distribution 🇺🇸 United States

TWINFIX/DURABRAID

DI: 03596010485663 · Model: 7210182 · Smith & Nephew, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
TWINFIX/DURABRAID
Primary DI
03596010485663
Version / Model
7210182
Catalog Number
7210182
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
8
Public Version Date
2025-07-07
Public Version Status
Update
Public Device Record Key
b65ef97d-f98b-4c5b-b673-15af62729f97
Distribution End Date
2022-03-17

Device Description

TWINFIX TI 3.5 SUTURE ANCHOR W/TWO 38

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

GMDN Terms

Code Name
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Primary 03596010485663

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K972326 000