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MCG Diagnostics

FDA UDI

Class II (US FDA UDI)

by Medical Graphics Corp.

Identity

Trade Name
MCG Diagnostics FDA UDI
Generic Name
Pulmonary function testing kit FDA UDI
Device Name
FILTER KIT 2 FDA UDI
Model / Reference
536723-001 FDA UDI
Description
FILTER KIT 2 FDA UDI

Identifiers

Catalog Number
536723-001 FDA UDI
Primary DI / UDI-DI
00810016250289 FDA UDI
510(k) Number
K042758 FDA UDI
FDA Product Code
BZG FDA UDI
GMDN Term
Pulmonary function testing kit 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulmonary function testing kit

MCG 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 kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20e79ec3-6476-46fa-abc7-c4a039d69da9 35 fields · synced May 30, 2026