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Ventiseal Oral/Nasal(on)et Tube Id 6.0 - Sterile -usa

FDA UDI

Class II (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
VENTISEAL ORAL/NASAL(ON)ET TUBE ID 6.0 - STERILE -USA FDA UDI
Generic Name
Basic endotracheal tube, single-use FDA UDI
Model / Reference
038-971-060U FDA UDI

Identifiers

Primary DI / UDI-DI
05055788728887 FDA UDI
FDA Product Code
BTR FDA UDI
GMDN Term
Basic endotracheal tube, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5730 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic endotracheal tube, single-use

Ventiseal Oral/Nasal(on)et Tube Id 6.0 - Sterile -usa by Flexicare Medical Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82cb12a1-95c8-4dae-9ef4-701adba9c8ec 32 fields · synced Jun 7, 2026