FDA UDI In Commercial Distribution 🇺🇸 United States

TenSURE

DI: 10840143901911 · Model: 80-02 · ATRICURE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
TenSURE
Primary DI
10840143901911
Version / Model
80-02
Catalog Number
FG-0017
Company Name
ATRICURE, INC.
Labeler DUNS
006133784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-11
Public Version
1
Public Version Date
2021-01-19
Public Version Status
New
Public Device Record Key
0108dfb7-b808-40c6-9618-1a64620610c3

Device Description

TenSURE Suture Tightener

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
Yes
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
FZT Cutter, Surgical

GMDN Terms

Code Name
47462 Suture knot-tying device

Identifiers

Type ID
Package 30840143901915
Primary 10840143901911
Package 50840143901896
Previous 00818354017618

Customer Contacts

Phone
650-354-1200