← Back to catalogue

Sontec Laryngoscope Set

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
SONTEC LARYNGOSCOPE SET FDA UDI
Generic Name
Laryngoscope handle, reusable FDA UDI
Device Name
SONTEC LARYNGOSCOPE SET MEDIUM SIZE FDA UDI
Model / Reference
485-315 FDA UDI
Description
SONTEC LARYNGOSCOPE SET MEDIUM SIZE FDA UDI

Identifiers

Catalog Number
485-315 FDA UDI
Primary DI / UDI-DI
00192896043633 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 Laryngoscope Set 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI 7c329920-20b7-4a9a-8787-3b1baf5f62ae 36 fields · synced May 30, 2026