Identity
- Trade Name
- Tensure FDA UDI
- Generic Name
- Suture/ligature tightener, single-use FDA UDI
- Device Name
- A sterile, manual, hand-held surgical device intended for controlled tightening of a ligature loop in situ (e.g., during vascular surgery). The ligature is intended to be loaded into the device, which typically includes a sliding mechanism, allowing controlled manual tightening; the device may also include tightening markers. This is a single-use device FDA UDI
- Model / Reference
- 7 lb FDA UDI
- Description
- A sterile, manual, hand-held surgical device intended for controlled tightening of a ligature loop in situ (e.g., during vascular surgery). The ligature is intended to be loaded into the device, which typically includes a sliding mechanism, allowing controlled manual tightening; the device may also include tightening markers. This is a single-use device FDA UDI
Identifiers
- Catalog Number
- 8002 FDA UDI
- Primary DI / UDI-DI
- M95580020 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Suture/ligature tightener, single-use 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/ligature tightener, single-use
Tensure by Sentreheart, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Suture/ligature tightener, single-use.
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- TACTIX Vector — Vilex, Inc. · Class I
- BOBsnare Device — LSI Solutions, Inc. · Class I
- miniRUMEL™ — LSI Solutions, Inc. · Class I
- RAPORT™ — LSI Solutions, Inc. · Class I
- RAPORT™ KIT — LSI Solutions, Inc. · Class I
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
- Sentreheart, Inc
Sources (1)
- FDA UDI 49e1a6e0-71a7-4c6d-a5de-0d09d8ad3233 35 fields · synced May 30, 2026