← Back to catalogue

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 blade FDA UDI
Device Name
S-VLB Laryngoscope Disposable blade FDA UDI
Model / Reference
S-VLB FDA UDI
Description
S-VLB Laryngoscope Disposable blade FDA UDI

Identifiers

Primary DI / UDI-DI
06974723790033 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Video intubation laryngoscope blade FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Category: Video intubation laryngoscope blade

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 blade.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI eb943458-31d8-4d19-98fa-50cbcf43e03f 34 fields · synced Jun 1, 2026