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Eclipse Pro, Defib Cable, Px, 3 Snap, Long

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 700-0390-00Model Eclipse Pro cables and patches

by Spacelabs Healthcare Ltd

Identity

Trade Name
ECLIPSE PRO,DEFIB CABLE,PX,3 SNAP,LONG EUDAMED
Eclipse Pro FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Eclipse Pro cables and patches EUDAMED
ECLIPSE PRO,DEFIB CABLE,PX,3 SNAP,LONG FDA UDI
Model / Reference
Eclipse Pro cables and patches EUDAMED
700-0390-00 EUDAMED
Eclipse Pro FDA UDI
Description
ECLIPSE PRO,DEFIB CABLE,PX,3 SNAP,LONG FDA UDI

Identifiers

Catalog Number
700-0390-00 FDA UDI
Primary DI / UDI-DI
10841522129674 EUDAMEDFDA UDI
Basic UDI-DI
08415221IEPROC&POWN7U EUDAMED
FDA Product Code
MWJ FDA UDI
EMDN Code
Z12050485 HOLTER SYSTEM INSTRUMENTS FOR CARDIOVASCULAR PARAMETERS - CONSUMABLES EUDAMED
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.2800 FDA UDI
Market of Registration
France 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Eclipse Pro, Defib Cable, Px, 3 Snap, Long by Spacelabs Healthcare Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
GB-MF-000001196
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED 80f5a181-7367-4ec5-96e9-afd5cb9c623c 61 fields · synced Aug 3, 2026
  • FDA UDI c7c03a17-b5b0-494b-a8a8-4fdd6547eea4 34 fields · synced May 30, 2026