Identity
- Trade Name
- Rico Suction Labs, Inc. FDA UDI
- Generic Name
- Surgical suction system FDA UDI
- Device Name
- Aspirator FDA UDI
- Model / Reference
- 1001 FDA UDI
- Description
- Aspirator FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00863110000403 FDA UDI
- FDA Product Code
- GCX FDA UDI
- GMDN Term
- Surgical suction system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- 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
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical suction system
Rico Suction Labs, Inc. by Rico Suction Labs Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Rico Suction Labs, Inc. — RICO SUCTION LABS INC · Class II
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 |
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Manufacturer
- Manufacturer
- Rico Suction Labs Inc
Sources (1)
- FDA UDI 92c96bc9-36e9-4a03-9678-d4c61e4c8b5c 34 fields · synced May 30, 2026