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SOS Shikani Optical Stylet, Adult

FDA UDI

Class II (US FDA UDI)

by Clarus Medical, Llc

Identity

Trade Name
SOS Shikani Optical Stylet, Adult FDA UDI
Generic Name
Flexible intubation laryngoscope, fibreoptic FDA UDI
Device Name
SOS Malleable Stylet, (Adult) FDA UDI
Model / Reference
30000-10 FDA UDI
Description
SOS Malleable Stylet, (Adult) FDA UDI

Identifiers

Catalog Number
30000-10 FDA UDI
Primary DI / UDI-DI
B06730000100 FDA UDI
FDA Product Code
EOB FDA UDI
GMDN Term
Flexible intubation laryngoscope, fibreoptic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4760 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
High-level Disinfectant FDA UDI

Category: Flexible intubation laryngoscope, fibreoptic

SOS Shikani Optical Stylet, Adult by Clarus Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible intubation laryngoscope, fibreoptic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Clarus Medical, Llc

Sources (1)

  • FDA UDI 202b4bb2-207c-4b80-84ec-32b5d0b4d249 35 fields · synced May 30, 2026