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Pleura Med

FDA UDI

Class II (US FDA UDI)

by Solomed, S.A. de C.V.

Identity

Trade Name
Pleura Med FDA UDI
Generic Name
Thoracic suction collection container FDA UDI
Device Name
Equipment to drain the pleural cavity FDA UDI
Model / Reference
Adult FDA UDI
Description
Equipment to drain the pleural cavity FDA UDI

Identifiers

Primary DI / UDI-DI
07500463968372 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Thoracic suction collection container 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

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

Yes

FDA UDI

Category: Thoracic suction collection container

Pleura Med by Solomed, S.A. de C.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thoracic suction collection container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Solomed, S.A. de C.V.

Sources (1)

  • FDA UDI d5343ff1-aff5-4284-9e26-fe7a14e72f3d 33 fields · synced May 30, 2026