FDA UDI In Commercial Distribution 🇺🇸 United States

ULTRABRAID

DI: 03596010511935 · Model: 7210915 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ULTRABRAID
Primary DI
03596010511935
Version / Model
7210915
Catalog Number
7210915
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
8
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
6be56fe4-8440-46a3-a543-5f75962937cb

Device Description

ULTRABRAID 2 COBRAID 38 LENGTH SINGL

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
GAT SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

GMDN Terms

Code Name
13907 Polyolefin/fluoropolymer suture, multifilament

Identifiers

Type ID
Package 23596010511939
Primary 03596010511935

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K041216 000