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Mini D-fend water trap

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 8002174

by GE Healthcare Finland Oy

Identity

Trade Name
NA FDA UDI
Generic Name
Breathing circuit condensate trap, single-use FDA UDI
Device Name
Mini D-fend water trap EUDAMED
MINI D-FEND WATER TRAP, 8002174 FDA UDI
Model / Reference
8002174 EUDAMED
Mini D-fend Water Trap, 8002174 FDA UDI
Description
MINI D-FEND WATER TRAP, 8002174 FDA UDI

Identifiers

Catalog Number
8002174 FDA UDI
Primary DI / UDI-DI
00840682102926 EUDAMEDFDA UDI
Basic UDI-DI
08406821BUG004787R EUDAMED
B-00840682102926 EUDAMED
510(k) Number
K052582 FDA UDI
FDA Product Code
BZK FDA UDI
CBS FDA UDI
BZL FDA UDI
CBQ FDA UDI
NHO FDA UDI
CBR FDA UDI
NHQ FDA UDI
NHP FDA UDI
CCL FDA UDI
CAP FDA UDI
EMDN Code
Z1203020285 MULTI-PARAMETER MONITORS - CONSUMABLES EUDAMED
GMDN Term
Breathing circuit condensate trap, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.1850 FDA UDI
868.1620 FDA UDI
868.1730 FDA UDI
868.1500 FDA UDI
868.1700 FDA UDI
868.1720 FDA UDI
868.2600 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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
MRI Safety
MR Unsafe FDA UDI

Category: General-purpose multi-parameter bedside monitor

Mini D-fend water trap by GE Healthcare Finland Oy — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
FI-MF-000001176

Sources (3)

  • EUDAMED 1a5b6201-684b-4d98-ba5a-102546d7e021 61 fields · synced Oct 6, 2026
  • EUDAMED bb97d411-7162-4745-a322-112a0ebfaa8c 61 fields · synced May 16, 2026
  • FDA UDI 3be9958c-1e4a-465b-8d56-705fe2c62309 36 fields · synced May 29, 2026