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Novalite

FDA UDI

Class I (US FDA UDI)

by Novamed-Usa

Identity

Trade Name
NOVALITE FDA UDI
Generic Name
Laryngoscope handle, reusable FDA UDI
Device Name
STD REUSABLE PENLIGHT LARYNGOSCOPE HANDLE - REQUIRING "AA" BATTERY FDA UDI
Model / Reference
14-600S-02 FDA UDI
Description
STD REUSABLE PENLIGHT LARYNGOSCOPE HANDLE - REQUIRING "AA" BATTERY FDA UDI

Identifiers

Primary DI / UDI-DI
00817499020897 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Laryngoscope handle, reusable 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Laryngoscope handle, reusable

Novalite by Novamed-Usa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope handle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novamed-Usa

Sources (1)

  • FDA UDI 01f33a57-4451-4ce4-8af9-560c53398fe0 34 fields · synced May 30, 2026