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SüpeVac – Portable Single Use Hand-Held Suction Device

FDA UDI

Class II (US FDA UDI)

by Gmmi Sdn. Bhd.

Identity

Trade Name
SüpeVac – Portable Single Use Hand-Held Suction Device FDA UDI
Generic Name
Emergency airway clearance suction system, pneumatic FDA UDI
Model / Reference
CM200 FDA UDI

Identifiers

Catalog Number
CM200 FDA UDI
Primary DI / UDI-DI
00860004198857 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Emergency airway clearance suction system, pneumatic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Emergency airway clearance suction system, pneumatic

SüpeVac – Portable Single Use Hand-Held Suction Device by Gmmi Sdn. Bhd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emergency airway clearance suction system, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gmmi Sdn. Bhd.

Sources (1)

  • FDA UDI 701139ce-f311-46dd-a917-8e41a7a55430 34 fields · synced May 31, 2026