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Sontec Operating Laryngoscope

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
SONTEC OPERATING LARYNGOSCOPE FDA UDI
Generic Name
Laryngoscope handle, reusable FDA UDI
Device Name
SONTEC OPERATING LARYNGOSCOPE SMALL SIZE FDA UDI
Model / Reference
485-1314 FDA UDI
Description
SONTEC OPERATING LARYNGOSCOPE SMALL SIZE FDA UDI

Identifiers

Catalog Number
485-1314 FDA UDI
Primary DI / UDI-DI
00192896080324 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

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

Category: Laryngoscope handle, reusable

Sontec Operating Laryngoscope by Sontec Instruments, Inc. — 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
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI 104c7310-e0db-4fbe-bc11-620519eb1b49 36 fields · synced May 30, 2026