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TV HD Wireless

FDA UDI

Class I (US FDA UDI)

by Baxter Medical Systems GmbH + Co. KG

Identity

Trade Name
TV HD Wireless FDA UDI
Generic Name
Surgical video camera FDA UDI
Device Name
TruVidia Wireless Receiver FDA UDI
Model / Reference
1940747 FDA UDI
Description
TruVidia Wireless Receiver FDA UDI

Identifiers

Primary DI / UDI-DI
00887761968240 FDA UDI
FDA Product Code
KQM FDA UDI
GMDN Term
Surgical video camera FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical video camera

TV HD Wireless by Baxter Medical Systems GmbH + Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical video camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c2765ab9-6d90-41fc-ab55-3e26bb58df92 34 fields · synced May 30, 2026