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Sensorendo

FDA UDI

Class I (US FDA UDI)

by Sensorendo Medical Technology (Zhuhai) Co., Ltd.

Identity

Trade Name
Sensorendo FDA UDI
Generic Name
Video intubation laryngoscope handle/monitor FDA UDI
Device Name
Flexible Video Laryngoscope Model S-FVL FDA UDI
Model / Reference
S-FVL FDA UDI
Description
Flexible Video Laryngoscope Model S-FVL FDA UDI

Identifiers

Primary DI / UDI-DI
06974723794413 FDA UDI
FDA Product Code
CAL FDA UDI
GMDN Term
Video intubation laryngoscope handle/monitor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5530 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Liquid Chemical FDA UDI

Category: Video intubation laryngoscope handle/monitor

Sensorendo by Sensorendo Medical Technology (Zhuhai) Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Video intubation laryngoscope handle/monitor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 31552173-3a76-4fb0-8269-0cc0baf6b00f 34 fields · synced May 29, 2026