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Cormix

FDA UDI

Class II (US FDA UDI)

by Metrix Company, The

Identity

Trade Name
CORMIX FDA UDI
Generic Name
Medication transfer set FDA UDI
Device Name
ONE LEG GRAVITY FILL SET With Female Screw Connector FDA UDI
Model / Reference
MS64794 FDA UDI
Description
ONE LEG GRAVITY FILL SET With Female Screw Connector FDA UDI

Identifiers

Catalog Number
MS64794 FDA UDI
Primary DI / UDI-DI
00812496011930 FDA UDI
510(k) Number
K030888 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Medication transfer set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medication transfer set

Cormix by Metrix Company, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medication transfer set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Metrix Company, The

Sources (1)

  • FDA UDI 53e671dc-ea04-499c-92eb-d8fe76cad784 36 fields · synced Jun 1, 2026