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Tracheal Intubation Fiberscope

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
TRACHEAL INTUBATION FIBERSCOPE FDA UDI
Generic Name
Flexible intubation laryngoscope, fibreoptic FDA UDI
Model / Reference
OLYMPUS LF-P FDA UDI

Identifiers

Catalog Number
N4447540 FDA UDI
Primary DI / UDI-DI
04953170452932 FDA UDI
510(k) Number
K221631 FDA UDI
FDA Product Code
EOQ FDA UDI
GMDN Term
Flexible intubation laryngoscope, fibreoptic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4680 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Flexible intubation laryngoscope, fibreoptic

Tracheal Intubation Fiberscope by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible intubation laryngoscope, fibreoptic.

Cleared under the same submission

K221631 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olympus Medical Systems Corporation

Sources (1)

  • FDA UDI 7c83fe0a-d3e4-44e3-a785-6e092c6ce171 35 fields · synced May 30, 2026