← Back to catalogue

GlideScope®

FDA UDI

Class I (US FDA UDI)

by Verathon Medical (Canada) ULC

Identity

Trade Name
GlideScope® FDA UDI
Generic Name
Video intubation laryngoscope blade FDA UDI
Device Name
GlideScope® Spectrum™ LoPro S2, Non-Sterile FDA UDI
Model / Reference
Spectrum™ LoPro S2, Non-Sterile FDA UDI
Description
GlideScope® Spectrum™ LoPro S2, Non-Sterile FDA UDI

Identifiers

Catalog Number
0574-0219 FDA UDI
Primary DI / UDI-DI
00879123002730 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Video intubation laryngoscope blade FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 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

Yes

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: Video intubation laryngoscope blade

GlideScope® by Verathon Medical (Canada) ULC — 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 d4ae7f1f-1906-4ee3-a12f-c2be8e938b74 34 fields · synced Jun 6, 2026