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Rescuer MVP Manual Vacuum Pump

FDA UDI

Class I (US FDA UDI)

by B.L.S. Systems Limited

Identity

Trade Name
Rescuer MVP Manual Vacuum Pump FDA UDI
Generic Name
Emergency airway clearance suction pump, manual FDA UDI
Device Name
Rescuer MVP Manual Vacuum Pump with Collection jar and two oral suction catheters FDA UDI
Model / Reference
7000-MVP FDA UDI
Description
Rescuer MVP Manual Vacuum Pump with Collection jar and two oral suction catheters FDA UDI

Identifiers

Catalog Number
7000-MVP FDA UDI
Primary DI / UDI-DI
B0027000MVP0 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Emergency airway clearance suction pump, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Emergency airway clearance suction pump, manual

Rescuer MVP Manual Vacuum Pump by B.L.S. Systems Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emergency airway clearance suction pump, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B.L.S. Systems Limited

Sources (1)

  • FDA UDI 61a1d355-3a39-4c40-9ac4-269b63d4f98f 36 fields · synced May 30, 2026