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Express

FDA UDI

Class II (US FDA UDI)

by Atrium Medical Corp.

Identity

Trade Name
EXPRESS FDA UDI
Generic Name
Negative-pressure wound therapy system pump, mechanical FDA UDI
Device Name
EXPRESS MINI 500 SUCTION BULB FDA UDI
Model / Reference
19930 FDA UDI
Description
EXPRESS MINI 500 SUCTION BULB FDA UDI

Identifiers

Primary DI / UDI-DI
00650862199307 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Negative-pressure wound therapy system pump, mechanical 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

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Category: Negative-pressure wound therapy system pump, mechanical

Express by Atrium Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system pump, mechanical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atrium Medical Corp.

Sources (1)

  • FDA UDI 22425828-1766-41f1-95e9-a4b7b5046dff 33 fields · synced May 30, 2026