Identity
- Trade Name
- EFFERGRIP ADHESIVE 2.5OZ TUBE 12 FDA UDI
- Generic Name
- Carboxymethylcellulose sodium denture adhesive FDA UDI
- Device Name
- EFFERGRIP ADHESIVE 2.5OZ TUBE 12 FDA UDI
- Model / Reference
- 10814832010314 FDA UDI
- Description
- EFFERGRIP ADHESIVE 2.5OZ TUBE 12 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00814832010317 FDA UDI
- FDA Product Code
- KOL FDA UDI
- GMDN Term
- Carboxymethylcellulose sodium denture adhesive FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3410 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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Carboxymethylcellulose sodium denture adhesive
Effergrip Adhesive 2.5oz Tube 12 by Medtech Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Carboxymethylcellulose sodium denture adhesive.
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- EFFERGRIP ADHESIVE 1.5OZ TUBE 24 — MEDTECH 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
- Medtech Products, Inc.
Sources (1)
- FDA UDI e986144b-3413-461d-bafd-56b1a7945415 34 fields · synced May 30, 2026