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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
Breathing circuit tube holder FDA UDI
Device Name
Hose clip 10mm x 3 FDA UDI
Model / Reference
900MR049 FDA UDI
Description
Hose clip 10mm x 3 FDA UDI

Identifiers

Catalog Number
900MR049 FDA UDI
Primary DI / UDI-DI
09420012401748 FDA UDI
FDA Product Code
JAY FDA UDI
GMDN Term
Breathing circuit tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5280 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breathing circuit tube holder

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 Breathing circuit tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e127373f-7252-4fab-8aca-baec16781c93 36 fields · synced May 30, 2026