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Zurich Medical Accessory Cable

FDA UDI

Class II (US FDA UDI)

by Zurich Medical

Identity

Trade Name
Zurich Medical Accessory Cable FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Model / Reference
Siemens 8-Pin, Type A FDA UDI

Identifiers

Catalog Number
512-141 FDA UDI
Primary DI / UDI-DI
00850022994265 FDA UDI
510(k) Number
K190852 FDA UDI
FDA Product Code
DSK FDA UDI
DQK FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1110 FDA UDI
870.1425 FDA UDI
Commercial Distribution
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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrical-only medical device connection cable, reusable

Zurich Medical Accessory Cable by Zurich Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zurich Medical

Sources (1)

  • FDA UDI 24fa26f9-301f-4aa5-99ce-8b2f5be6dd62 34 fields · synced Jun 6, 2026