InspiraChamber® 100110

by Flexicare Medical Limited

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number05023323029751 UDI-DI	Date17 May 2024Listed	StatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: InspiraChamber®
Generic Name: Medicine chamber spacer, reusable
Model / Reference: 100110

Primary DI / UDI-DI: 05023323029751
FDA Product Code: NVP
GMDN Term: Medicine chamber spacer, reusable

Device Class: Class II
Regulation Number: 868.5630
GUDID distribution status: Not in Commercial Distribution

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Properties

Prescription Use
Lot / Batch Number
Manufacturing Date

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Expiration Date: No