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Newport Medical

FDA UDI

Class I (US FDA UDI)

by Newport Medical Instruments

Identity

Trade Name
Newport Medical FDA UDI
Generic Name
Ventilator breathing circuit, reusable FDA UDI
Device Name
Universal Ventilation Breathing Circuit FDA UDI
Model / Reference
BCD32820P FDA UDI
Description
Universal Ventilation Breathing Circuit FDA UDI

Identifiers

Primary DI / UDI-DI
10884521540583 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Ventilator breathing circuit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Newport Medical by Newport Medical Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1265546d-76d1-4ece-9f64-519fd196d22d 36 fields · synced May 30, 2026