Identity
- Trade Name
- ViveCare FDA UDI
- Generic Name
- Skin surface device adhesive FDA UDI
- Device Name
- Ostomy Adhesive Barrier (10PK) FDA UDI
- Model / Reference
- LVA3054CT10 FDA UDI
- Description
- Ostomy Adhesive Barrier (10PK) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810113577142 FDA UDI
- FDA Product Code
- EXE FDA UDI
- GMDN Term
- Skin surface device adhesive FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5900 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Skin surface device adhesive
ViveCare by Vive Health Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Skin surface device adhesive.
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- Uro-Bond® V Brush-On Non-Flammable Silicone Adhesive 1.5 oz. (44.4 mL.) — UROCARE PRODUCTS, INC. · Class I
- Urofoam®-2 Double-Sided Adhesive Foam Strip Box of 50 — UROCARE PRODUCTS, 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
- Vive Health Llc
Sources (1)
- FDA UDI d3288c15-c5a1-42d8-a692-0c6df915201b 33 fields · synced May 31, 2026