← Back to catalogue

Molded Products, Inc

FDA UDI

Class II (US FDA UDI)

by Molded Products Inc.

Identity

Trade Name
Molded Products, Inc FDA UDI
Generic Name
Luer-formatted disinfection cap FDA UDI
Device Name
Latex-Free Access Site with Luer Slip FDA UDI
Model / Reference
MPC-100-S FDA UDI
Description
Latex-Free Access Site with Luer Slip FDA UDI

Identifiers

Catalog Number
MPC-100-S FDA UDI
Primary DI / UDI-DI
B144MPC100S0 FDA UDI
510(k) Number
K925927 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Luer-formatted disinfection cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luer-formatted disinfection cap

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

Similar devices

Also classified as Luer-formatted disinfection cap.

Cleared under the same submission

K925927 also covers:

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
Molded Products Inc.

Sources (1)

  • FDA UDI 10d96ecc-a706-4fec-8418-d274a159aed9 35 fields · synced May 30, 2026