← Back to catalogue

Immy

FDA UDI

Class I (US FDA UDI)

by Immuno-Mycologics, Inc.

Identity

Trade Name
IMMY FDA UDI
Generic Name
Sputum liquefaction/decontamination reagent IVD FDA UDI
Device Name
MycoDDR 3.0% NaOH Reagent Kit FDA UDI
Model / Reference
DDR012-3.0 FDA UDI
Description
MycoDDR 3.0% NaOH Reagent Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00816387020995 FDA UDI
FDA Product Code
PPM FDA UDI
GMDN Term
Sputum liquefaction/decontamination reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sputum liquefaction/decontamination reagent IVD

Immy by Immuno-Mycologics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sputum liquefaction/decontamination reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Immuno-Mycologics, Inc.

Sources (1)

  • FDA UDI 56c18583-6d21-4f2b-9fee-5e8766a6e905 34 fields · synced May 30, 2026