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Inspire

FDA UDI

Class I (US FDA UDI)

by Inspiration Healthcare, Ltd.

Identity

Trade Name
Inspire FDA UDI
Generic Name
Anaesthesia mask strap, reusable FDA UDI
Device Name
IHC608 INSPIRE nCPAP Spare Ribbon FDA UDI
Model / Reference
IHC608 FDA UDI
Description
IHC608 INSPIRE nCPAP Spare Ribbon FDA UDI

Identifiers

Primary DI / UDI-DI
05060206920149 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Anaesthesia mask strap, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia mask strap, reusable

Inspire by Inspiration Healthcare, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia mask strap, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c76ab5b2-1773-4823-a8c1-d90598b847e0 34 fields · synced May 30, 2026