← Back to catalogue

M'Ath

FDA UDI

Class II (US FDA UDI)

by I M T

Identity

Trade Name
M'Ath FDA UDI
Generic Name
Cardiovascular risk evaluation interpretive software FDA UDI
Model / Reference
3.2.1 SR FDA UDI

Identifiers

Primary DI / UDI-DI
03760264690061 FDA UDI
510(k) Number
K040686 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Cardiovascular risk evaluation interpretive software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiovascular risk evaluation interpretive software

M'Ath by I M T — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiovascular risk evaluation interpretive software.

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
I M T

Sources (1)

  • FDA UDI 3d4ce77a-b816-4221-8da6-06a7cebd40a9 33 fields · synced Jun 6, 2026