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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
Vascular puncture haemostasis arm clamp/band, reusable FDA UDI
Device Name
Fistula Pressure Clamp 'Ultra Grip' Cover FDA UDI
Model / Reference
MPC-255 FDA UDI
Description
Fistula Pressure Clamp 'Ultra Grip' Cover FDA UDI

Identifiers

Catalog Number
MPC-255 FDA UDI
Primary DI / UDI-DI
B144MPC2551 FDA UDI
FDA Product Code
NOO FDA UDI
GMDN Term
Vascular puncture haemostasis arm clamp/band, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5540 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

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

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: Vascular puncture haemostasis arm clamp/band, 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 Vascular puncture haemostasis arm clamp/band, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 98d1fb99-ab5a-4648-a307-99080d49e53a 34 fields · synced May 31, 2026