BaseVac

FDA UDI

Class I (US FDA UDI)

by R. E. Morrison Equipment Inc

Identity

Trade Name: BaseVac FDA UDI
Generic Name: Dental suction system FDA UDI
Device Name: 2.5 User All-In-One Vacuum w/ Integrated Air Water Separator FDA UDI
Model / Reference: 2M4.25-230 FDA UDI
Description: 2.5 User All-In-One Vacuum w/ Integrated Air Water Separator FDA UDI

Identifiers

Catalog Number: 2800026 FDA UDI
Primary DI / UDI-DI: D13028000260 FDA UDI
FDA Product Code: NRD FDA UDI
GMDN Term: Dental suction system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.6640 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental suction system

BaseVac by R. E. Morrison Equipment Inc — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: R. E. Morrison Equipment Inc

Sources (1)

FDA UDI a8704a97-0851-4c85-b858-c598281bb4ee 35 fields · synced Jun 8, 2026