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ProCure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
ProCure FDA UDI
Generic Name
Tracheostomy care kit, single-use FDA UDI
Device Name
Tracheostomy Care Kit 1-Compartment Tray Sterile FDA UDI
Model / Reference
1006350 FDA UDI
Description
Tracheostomy Care Kit 1-Compartment Tray Sterile FDA UDI

Identifiers

Catalog Number
1006350 FDA UDI
Primary DI / UDI-DI
10840330704240 FDA UDI
FDA Product Code
LRQ FDA UDI
GMDN Term
Tracheostomy care kit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tracheostomy care kit, single-use

ProCure by Twin Med, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostomy care kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Twin Med, LLC

Sources (1)

  • FDA UDI f329aa56-d047-444a-be4c-c0d23d9f1bc2 35 fields · synced Jun 1, 2026