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Max Pro Medical Freeze Spray

FDA UDI

Class I (US FDA UDI)

by Ecotec Manufacturing

Identity

Trade Name
Max Pro Medical Freeze Spray FDA UDI
Generic Name
Cryogenic tissue spray IVD FDA UDI
Device Name
Medical Freeze Spray FDA UDI
Model / Reference
MPMF-6567 FDA UDI
Description
Medical Freeze Spray FDA UDI

Identifiers

Primary DI / UDI-DI
00860177000636 FDA UDI
FDA Product Code
IFI FDA UDI
GMDN Term
Cryogenic tissue spray 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Category: Cryogenic tissue spray IVD

Max Pro Medical Freeze Spray by Ecotec Manufacturing — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cryogenic tissue spray IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e25a9c07-a77c-4392-966c-3fb877913466 33 fields · synced Jun 1, 2026