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Molded Products, Inc.

FDA UDI

Class I (US FDA UDI)

by Molded Products Inc.

Identity

Trade Name
Molded Products, Inc. FDA UDI
Generic Name
Medical tubing clip/clamp, temporary, non-calibrated, reusable FDA UDI
Device Name
Premium Tube Occluding Forcep - Blue - 10/Pk FDA UDI
Model / Reference
MPC-225-10 FDA UDI
Description
Premium Tube Occluding Forcep - Blue - 10/Pk FDA UDI

Identifiers

Catalog Number
MPC-225-10 FDA UDI
Primary DI / UDI-DI
B144MPC225105 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Medical tubing clip/clamp, temporary, non-calibrated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Medical tubing clip/clamp, temporary, non-calibrated, reusable

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

Similar devices

Also classified as Medical tubing clip/clamp, temporary, non-calibrated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 33d3fe70-cdf3-49d4-9345-9bcb6f76b8d9 34 fields · synced May 30, 2026