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Classic RT

FDA UDI

Class I (US FDA UDI)

by Plastiflex Group NV

Identity

Trade Name
Classic RT FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Model / Reference
Classic RT 19 x 1200 White FDA UDI

Identifiers

Primary DI / UDI-DI
05404013002177 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 FDA UDI
Commercial Distribution
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

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: Ventilator breathing circuit, single-use

Classic RT by Plastiflex Group NV — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plastiflex Group NV

Sources (1)

  • FDA UDI 9eaabf8d-6534-43bf-a208-d872e514c250 32 fields · synced May 31, 2026