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Spacelabs Healthcare

FDA UDI

Class II (US FDA UDI)

by Spacelabs Healthcare (washington), Inc

Identity

Trade Name
Spacelabs Healthcare FDA UDI
Generic Name
Electrocardiograph, professional, multichannel FDA UDI
Device Name
HOOKUP SET-53 NON-DISPOSABLE ELECTRODE FDA UDI
Model / Reference
CDIRECT; CD12USB; CCOLLECT FDA UDI
Description
HOOKUP SET-53 NON-DISPOSABLE ELECTRODE FDA UDI

Identifiers

Catalog Number
41-0053US FDA UDI
Primary DI / UDI-DI
10841522125911 FDA UDI
FDA Product Code
DPS FDA UDI
GMDN Term
Electrocardiograph, professional, multichannel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2340 FDA UDI
Commercial Distribution
Not 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Spacelabs Healthcare by Spacelabs Healthcare (washington), Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e368af90-b99f-4194-816f-bdacde80cbcc 35 fields · synced May 31, 2026