Low Pressure Connector Tubing

FDA UDI

Class II (US FDA UDI)

by Bayer Medical Care Inc.

Identity

Trade Name: Low Pressure Connector Tubing FDA UDI
Generic Name: Radiographic procedure tubing FDA UDI
Device Name: Envision, Vistron, MCT - Coiled 60" Low Pressure Connector Tube (SET, PKG, LPDCT 160, RAD, MC) (60728885) FDA UDI
Model / Reference: LPDCT 160 FDA UDI
Description: Envision, Vistron, MCT - Coiled 60" Low Pressure Connector Tube (SET, PKG, LPDCT 160, RAD, MC) (60728885) FDA UDI

Identifiers

Catalog Number: LPDCT 160 FDA UDI
Primary DI / UDI-DI: 00616258005638 FDA UDI
FDA Product Code: DOY FDA UDI
GMDN Term: Radiographic procedure tubing FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 862.3320 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiographic procedure tubing

Low Pressure Connector Tubing by Bayer Medical Care Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Bayer Medical Care Inc.

Sources (1)

FDA UDI 89ce51b2-eb74-4bdc-af30-126cbf351519 35 fields · synced Jun 9, 2026