Identity
- Trade Name
- Expression MR KIT,DISPOSABLE WATER TRAP,3160 FDA UDI
- Generic Name
- Breathing circuit condensate trap, reusable FDA UDI
- Model / Reference
- Kit, Disposable Water Trap, 3160 FDA UDI
Identifiers
- Catalog Number
- 94012 FDA UDI
- Primary DI / UDI-DI
- 00884838016057 FDA UDI
- FDA Product Code
- MWI FDA UDI
- GMDN Term
- Breathing circuit condensate trap, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2300 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
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
Category: Breathing circuit condensate trap, reusable
Expression MR KIT, DISPOSABLE WATER TRAP, 3160 by Philips DS North America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 59845d0e-518c-43ee-b06f-6bf0ae281b53 34 fields · synced Jun 8, 2026