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Dispiro

FDA UDI

Class II (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
DISPIRO FDA UDI
Generic Name
Gasometer FDA UDI
Device Name
22 MM CONNECTOR W/ ONE-WAY VALVE FDA UDI
Model / Reference
22mm Connector FDA UDI
Description
22 MM CONNECTOR W/ ONE-WAY VALVE FDA UDI

Identifiers

Catalog Number
02040 FDA UDI
Primary DI / UDI-DI
H671020401 FDA UDI
510(k) Number
K791177 FDA UDI
FDA Product Code
BZG FDA UDI
GMDN Term
Gasometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1840 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 22 Millimeter FDA UDI

Category: Gasometer

Dispiro by Utah Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gasometer.

Cleared under the same submission

K791177 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Utah Medical Products, Inc.

Sources (1)

  • FDA UDI c0d76a51-cedb-4b49-99d8-f4fe8b5084af 37 fields · synced Jun 9, 2026