Identity
- Trade Name
- Mermaid Medical FDA UDI
- Generic Name
- Wearable percutaneous catheter/tube holder FDA UDI
- Device Name
- Mermaid Medical Specialty Securement Device - Drainage Tube White Loop/Liner/Hook/Foam/Bandage Sterile Extra Small FDA UDI
- Model / Reference
- A20100090 FDA UDI
- Description
- Mermaid Medical Specialty Securement Device - Drainage Tube White Loop/Liner/Hook/Foam/Bandage Sterile Extra Small FDA UDI
Identifiers
- Catalog Number
- A20100090 FDA UDI
- Primary DI / UDI-DI
- 28481750004016 FDA UDI
- FDA Product Code
- KMK FDA UDI
- GMDN Term
- Wearable percutaneous catheter/tube holder FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5210 FDA UDI
- Commercial Distribution
- Not 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Mermaid Medical by Tidi Products, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Tidi Products, Llc
Sources (1)
- FDA UDI 3bc28cf1-0977-4af5-8cc0-a96dbd0d9d4f 35 fields · synced Jun 6, 2026