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Sensorendo

FDA UDIEUDAMED

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
Single Use Flexible Video Laryngoscope Model S-DVL FDA UDI
Model / Reference
S-DVL FDA UDI
Description
Single Use Flexible Video Laryngoscope Model S-DVL FDA UDI

Identifiers

Primary DI / UDI-DI
06974723796011 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
Ethylene Oxide FDA UDI

Category: Video intubation laryngoscope handle/monitor

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

Similar devices

Also classified as Video intubation laryngoscope handle/monitor.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 03f03671-86b1-4072-a906-c0031c2da45a 34 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced May 29, 2026