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Fisher & Paykel Healthcare

FDA UDI

Class I (US FDA UDI)

by Fisher & Paykel Healthcare, Inc.

Identity

Trade Name
Fisher & Paykel Healthcare FDA UDI
Generic Name
Inspiratory/expiratory limb respiratory tubing, reusable FDA UDI
Device Name
Inlet Tube - HC150 0.6M FDA UDI
Model / Reference
900HC008 FDA UDI
Description
Inlet Tube - HC150 0.6M FDA UDI

Identifiers

Catalog Number
900HC008 FDA UDI
Primary DI / UDI-DI
09420012400567 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Inspiratory/expiratory limb respiratory tubing, reusable 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Category: Inspiratory/expiratory limb respiratory tubing, reusable

Fisher & Paykel Healthcare by Fisher & Paykel Healthcare, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inspiratory/expiratory limb respiratory tubing, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fisher & Paykel Healthcare, Inc.

Sources (1)

  • FDA UDI fd637668-333c-437e-bb1d-f2baa6582b55 35 fields · synced May 30, 2026