FDA UDI In Commercial Distribution 🇺🇸 United States

TenSURE

DI: 10840143909696 · Model: 80-02 · ATRICURE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
TenSURE
Primary DI
10840143909696
Version / Model
80-02
Catalog Number
FG-0017-02
Company Name
ATRICURE, INC.
Labeler DUNS
006133784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-06
Public Version
1
Public Version Date
2023-04-14
Public Version Status
New
Public Device Record Key
8b839b21-56a3-48c0-89b1-476d38a7defe

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
MR Safe
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
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
47462 Suture knot-tying device

Identifiers

Type ID
Package 30840143909683
Primary 10840143909696
Package 50840143909687

Customer Contacts

Phone
866-449-2342

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place