Identity
- Trade Name
- Grip-Lok FDA UDI
- Generic Name
- Wearable percutaneous catheter/tube holder FDA UDI
- Device Name
- Grip-Lok WA Medium,Universal Catheter Securement Device with Aplicare P-1010 Skin Prep Pad FDA UDI
- Model / Reference
- 3360MWA FDA UDI
- Description
- Grip-Lok WA Medium,Universal Catheter Securement Device with Aplicare P-1010 Skin Prep Pad FDA UDI
Identifiers
- Catalog Number
- 3360MWA FDA UDI
- Primary DI / UDI-DI
- 00618125134533 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Grip-Lok 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 |
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Manufacturer
- Manufacturer
- Tidi Products, Llc
Sources (1)
- FDA UDI 0bd319ce-4cbf-4992-8f67-12fb3998fe3e 35 fields · synced May 30, 2026