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Toad

FDA UDI

Class I (US FDA UDI)

by Wm&Dg

Identity

Trade Name
TOAD FDA UDI
Generic Name
Channelled video intubation laryngoscope FDA UDI
Device Name
S-VLB disposable laryngoscope blade non-sterile FDA UDI
Model / Reference
S-VLB FDA UDI
Description
S-VLB disposable laryngoscope blade non-sterile FDA UDI

Identifiers

Primary DI / UDI-DI
00850027060026 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Channelled video intubation laryngoscope 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

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Channelled video intubation laryngoscope

Toad by Wm&Dg — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Channelled video intubation laryngoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wm&Dg

Sources (1)

  • FDA UDI 57f9cbee-1f78-4902-85cc-54d458be6ccb 33 fields · synced May 30, 2026