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NMT Sensor Cable, 3, 3 m

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 888414

by GE Healthcare Finland Oy

Identity

Trade Name
NA FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
NMT Sensor Cable, 3,3 m EUDAMED
NMT Sensor Cable EUDAMED
NMT SENSOR CABLE 3.3M/11FT, 888414 FDA UDI
Model / Reference
888414 EUDAMED
NMT Sensor Cable 3.3m/11ft, 888414 FDA UDI
Description
NMT SENSOR CABLE 3.3M/11FT, 888414 FDA UDI

Identifiers

Catalog Number
888414 FDA UDI
Primary DI / UDI-DI
00840682103503 EUDAMEDFDA UDI
Basic UDI-DI
B-00840682103503 EUDAMED
08406821BUG004857N EUDAMED
Direct Marketing DI
00840682103503 EUDAMED
510(k) Number
K051635 FDA UDI
FDA Product Code
KOI FDA UDI
EMDN Code
Z1203020280 MULTI-PARAMETER MONITORS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I EUDAMED
Class II FDA UDI
Regulation Number
868.2775 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

NMT Sensor Cable, 3, 3 m by GE Healthcare Finland Oy — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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 0c4f73ff-585a-49b9-96a1-3bef732f1cca 61 fields · synced Oct 6, 2026
  • EUDAMED ed754c8d-4549-4630-b9ea-08391224fd74 61 fields · synced May 17, 2026
  • FDA UDI b7702470-5531-4f0a-bb88-bb806161a50b 37 fields · synced May 30, 2026