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MGC Diagnostics

FDA UDI

Class II (US FDA UDI)

by Medical Graphics Corp.

Identity

Trade Name
MGC Diagnostics FDA UDI
Generic Name
Pulmonary function testing filter/mouthpiece FDA UDI
Device Name
DIRECTCONNECT FLOW SENSOR NON-KEYED FDA UDI
Model / Reference
750050-003 FDA UDI
Description
DIRECTCONNECT FLOW SENSOR NON-KEYED FDA UDI

Identifiers

Catalog Number
750050-003 FDA UDI
Primary DI / UDI-DI
00810016250814 FDA UDI
FDA Product Code
JAX FDA UDI
GMDN Term
Pulmonary function testing filter/mouthpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2550 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

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: Pulmonary function testing filter/mouthpiece

MGC Diagnostics by Medical Graphics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function testing filter/mouthpiece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eaa6a890-68b9-4de1-9da6-8074f6f74cd2 34 fields · synced Jun 1, 2026