Identity
- Trade Name
- APack Watertrap Adult FDA UDI
- Generic Name
- Microbial medical gas filter, single-use FDA UDI
- Model / Reference
- MP01682 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04048675420989 FDA UDI
- FDA Product Code
- CAI FDA UDI
- GMDN Term
- Microbial medical gas filter, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5240 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Anaesthesia breathing circuit, single-useGas-sampling/monitoring respiratory tubing, single-useMicrobial medical gas filter, single-useBreathing circuit bag, single-use
APack Watertrap Adult by Drägerwerk AG & Co. KGaA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Breathing circuit bag, single-use.
- BREATHING BAG — KING SYSTEMS CORPORATION. · Class I
- Breathing bags — Shandong Jinlai Huanhai Medical Technology Co., Ltd. · Class I
- 2 LITER CONTOUR® — KING SYSTEMS CORPORATION. · Class I
- Halyard Breathing Bag — Airlife, Inc. · Class I
- Breathing bags — Shandong Jinlai Huanhai Medical Technology Co., Ltd. · Class I
- Breathing bags — Shandong Jinlai Huanhai Medical Technology Co., Ltd. · Class I
- Breathing bag anest disp 1L compl — Maquet Critical Care AB · Class I
- Bag, Breathing, 3-Liter Latex Free — A-M Systems, Inc. · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Drägerwerk AG & Co. KGaA
Sources (1)
- FDA UDI adeb2c76-d601-42af-bb0e-d7cf967f01c6 33 fields · synced May 30, 2026