Identity
- Trade Name
- TenSURE FDA UDI
- Generic Name
- Suture knot-tying device FDA UDI
- Device Name
- TenSURE Suture Tightener FDA UDI
- Model / Reference
- 80-02 FDA UDI
- Description
- TenSURE Suture Tightener FDA UDI
Identifiers
- Catalog Number
- FG-0017 FDA UDI
- Primary DI / UDI-DI
- 10840143901911 FDA UDI
- FDA Product Code
- FZT FDA UDI
- GMDN Term
- Suture knot-tying device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Suture knot-tying device
TenSURE by Atricure, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Atricure, Inc.
Sources (1)
- FDA UDI 0108dfb7-b808-40c6-9618-1a64620610c3 35 fields · synced May 31, 2026