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Ultrasound Transducer

FDA UDI

Class II (US FDA UDI)

by Wipro GE Healthcare Private Ltd

Identity

Trade Name
ULTRASOUND TRANSDUCER FDA UDI
Generic Name
Foetal/maternal prenatal monitor FDA UDI
Model / Reference
NA FDA UDI

Identifiers

Catalog Number
2108346 FDA UDI
Primary DI / UDI-DI
00840682142564 FDA UDI
510(k) Number
K982651 FDA UDI
FDA Product Code
HEL FDA UDI
GMDN Term
Foetal/maternal prenatal monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2660 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: Foetal/maternal prenatal monitor

Ultrasound Transducer by Wipro GE Healthcare Private Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foetal/maternal prenatal monitor.

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 30c96f60-b1e9-4eba-9357-4a3066f3bb0f 36 fields · synced Jun 8, 2026