Identity
- Trade Name
- Expression MR KIT,WATER TRAP,ETCO2,3160 FDA UDI
- Generic Name
- Breathing circuit condensate trap, reusable FDA UDI
- Device Name
- KIT,WATER TRAP,ETCO2,3160 FDA UDI
- Model / Reference
- Kit, Water Trap, EtCO2, 3160 FDA UDI
- Description
- KIT,WATER TRAP,ETCO2,3160 FDA UDI
Identifiers
- Catalog Number
- 94020 FDA UDI
- Primary DI / UDI-DI
- 00884838045132 FDA UDI
- FDA Product Code
- CCK FDA UDI
- GMDN Term
- Breathing circuit condensate trap, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1400 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Expression MR KIT, WATER TRAP, ETCO2, 3160 by Philips DS North America LLC — 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 |
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Manufacturer
- Manufacturer
- Philips DS North America LLC
Sources (1)
- FDA UDI 7b50fa77-77f4-4bbc-84a8-671d028596ed 36 fields · synced Jun 8, 2026