Identity
- Trade Name
- Tridyne FDA UDI
- Generic Name
- Surgical internal adhesive/sealant, human-derived FDA UDI
- Device Name
- Tridyne, Vascular Sealant, Kit FDA UDI
- Model / Reference
- TDVS004 FDA UDI
- Description
- Tridyne, Vascular Sealant, Kit FDA UDI
Identifiers
- Catalog Number
- TDVS004 FDA UDI
- Primary DI / UDI-DI
- 00801741099366 FDA UDI
- FDA Product Code
- NBE FDA UDI
- GMDN Term
- Surgical internal adhesive/sealant, human-derived FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 4 Milliliter FDA UDI
Category: Surgical internal adhesive/sealant, human-derived
Tridyne by Neomend, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical internal adhesive/sealant, human-derived.
- Progel — Neomend, Inc. · Class III
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 III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Neomend, Inc.
Sources (1)
- FDA UDI 5d81d919-c4a7-4937-8ba8-9fad157e6221 37 fields · synced Jun 8, 2026