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Fisher & Paykel Healthcare

FDA UDI

Class II (US FDA UDI)

by Fisher & Paykel Healthcare, Inc.

Identity

Trade Name
Fisher & Paykel Healthcare FDA UDI
Generic Name
Insufflation gas conditioning system control unit FDA UDI
Device Name
HUMIDIFIER SH870 115V US FDA UDI
Model / Reference
SH870JHU FDA UDI
Description
HUMIDIFIER SH870 115V US FDA UDI

Identifiers

Catalog Number
SH870JHU FDA UDI
Primary DI / UDI-DI
09420012433060 FDA UDI
FDA Product Code
HIF FDA UDI
GMDN Term
Insufflation gas conditioning system control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1730 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Insufflation gas conditioning system control unit

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

Similar devices

Also classified as Insufflation gas conditioning system control unit.

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 6df25a3c-e6ce-49a3-892d-5408bfb9c3ac 36 fields · synced May 31, 2026