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Molded Products, Inc.

FDA UDI

Class II (US FDA UDI)

by Molded Products Inc.

Identity

Trade Name
Molded Products, Inc. FDA UDI
Generic Name
Haemodialysis system dialysate delivery set FDA UDI
Device Name
Male to Male Recirculation Connector FDA UDI
Model / Reference
MPC-825 FDA UDI
Description
Male to Male Recirculation Connector FDA UDI

Identifiers

Catalog Number
MPC-825 FDA UDI
Primary DI / UDI-DI
B144MPC8251 FDA UDI
510(k) Number
K010712 FDA UDI
FDA Product Code
FID FDA UDI
GMDN Term
Haemodialysis system dialysate delivery set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haemodialysis system dialysate delivery set

Molded Products, Inc. by Molded Products Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis system dialysate delivery set.

Cleared under the same submission

K010712 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Molded Products Inc.

Sources (1)

  • FDA UDI 6879ac6a-8578-4f54-9b96-e8f02a21d91b 35 fields · synced Jun 8, 2026