← Back to catalogue

My Medical

FDA UDI

Class I (US FDA UDI)

by My Medical Store Llc

Identity

Trade Name
My Medical FDA UDI
Generic Name
Laryngectomy tube FDA UDI
Device Name
Yankauer suction tube 5mm FDA UDI
Model / Reference
600-625 FDA UDI
Description
Yankauer suction tube 5mm FDA UDI

Identifiers

Catalog Number
600-625 FDA UDI
Primary DI / UDI-DI
G425MM6006250 FDA UDI
FDA Product Code
JZF FDA UDI
GMDN Term
Laryngectomy tube 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Laryngectomy tube

My Medical by My Medical Store Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngectomy tube.

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
My Medical Store Llc

Sources (1)

  • FDA UDI b7b3a5c2-47dc-43d5-82e6-cdcc09a39368 34 fields · synced Jun 8, 2026