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Single-Use Flexible Rhinolaryngoscope

FDA UDI

Class II (US FDA UDI)

by Hunan Vathin Medical Instrument Co., Ltd

Identity

Trade Name
Single-Use Flexible Rhinolaryngoscope FDA UDI
Generic Name
Flexible video otorhinolaryngoscope, single-use FDA UDI
Model / Reference
RL-S1800 FDA UDI

Identifiers

Primary DI / UDI-DI
06972197480795 FDA UDI
510(k) Number
K221581 FDA UDI
FDA Product Code
EOB FDA UDI
GMDN Term
Flexible video otorhinolaryngoscope, single-use 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Flexible video otorhinolaryngoscope, single-use

Single-Use Flexible Rhinolaryngoscope by Hunan Vathin Medical Instrument Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video otorhinolaryngoscope, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a1dd1632-47f8-4a7a-981d-d9bef5d46c04 33 fields · synced May 30, 2026