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Mini Telemetry System

FDA UDI

Class II (US FDA UDI)

by Wipro GE Healthcare Private Ltd

Identity

Trade Name
Mini Telemetry System FDA UDI
Generic Name
Cardiotocography telemetric monitoring system FDA UDI
Model / Reference
2051444-002 FDA UDI

Identifiers

Primary DI / UDI-DI
00840682117081 FDA UDI
510(k) Number
K110556 FDA UDI
FDA Product Code
HGM FDA UDI
GMDN Term
Cardiotocography telemetric monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2740 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiotocography telemetric monitoring system

Mini Telemetry System by Wipro GE Healthcare Private Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiotocography telemetric monitoring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d6b3d331-ceb1-476c-8093-5cd8476da091 34 fields · synced May 30, 2026