← Back to catalogue

Heermann Endolaryngeal Handle

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
HEERMANN ENDOLARYNGEAL HANDLE FDA UDI
Generic Name
Laryngoscope handle, reusable FDA UDI
Device Name
HEERMANN ENDOLARYNGEAL HANDLE UNIVERSAL BLACK COATED FDA UDI
Model / Reference
1301-549 FDA UDI
Description
HEERMANN ENDOLARYNGEAL HANDLE UNIVERSAL BLACK COATED FDA UDI

Identifiers

Catalog Number
1301-549 FDA UDI
Primary DI / UDI-DI
00192896096714 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Laryngoscope handle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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 — 5.25 Inch FDA UDI

Category: Laryngoscope handle, reusable

Heermann Endolaryngeal Handle 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 31a80b6a-9872-4d6a-b39f-fa38b1cefe49 36 fields · synced Jun 8, 2026