Identity
- Trade Name
- DRAIN-CADDY FDA UDI
- Generic Name
- Suction system container stand FDA UDI
- Device Name
- DRAIN CADDY (Drain Accessories) FDA UDI
- Model / Reference
- 19911 FDA UDI
- Description
- DRAIN CADDY (Drain Accessories) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00650862199116 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Suction system container stand FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Drain-Caddy by Atrium Medical Corp. — Class II — 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Atrium Medical Corp.
Sources (1)
- FDA UDI 5b5874a8-8234-4c6f-b70e-e2676b552cbf 34 fields · synced Jun 8, 2026