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Vide

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref ST382-0001

by Alleva Medical, Ltd.

Identity

Trade Name
Vide® Disposable Dry Suction/Dry Seal Chest Drainage EUDAMED
Vide FDA UDI
Generic Name
Thoracic suction collection container FDA UDI
Device Name
Vide® Disposable Dry Suction/Dry Seal Chest Drainage EUDAMED
Vide Sand Dry Seal Chest Drain FDA UDI
Model / Reference
ST382-0001 EUDAMEDFDA UDI
Description
Vide Sand Dry Seal Chest Drain FDA UDI

Identifiers

Catalog Number
ST382-0001 FDA UDI
Primary DI / UDI-DI
04897089070392 EUDAMEDFDA UDI
Basic UDI-DI
489708907ST382Q4 EUDAMED
Direct Marketing DI
04897089070392 EUDAMED
FDA Product Code
KDQ FDA UDI
EMDN Code
A0601010201 DRAINAGE SYSTEMS WITH ADJUSTABLE SUCTION AND COLLECTION CHAMBER EUDAMED
GMDN Term
Thoracic suction collection container FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Thoracic suction collection container

Vide by Alleva Medical, Ltd. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Thoracic suction collection container.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Alleva Medical, Ltd.

Sources (2)

  • FDA UDI 301f5122-6c30-4a16-a62b-580fc5b36404 34 fields · synced Jun 18, 2026
  • EUDAMED c42aadea-e761-4334-9496-7d03a18feb17 61 fields · synced Jun 18, 2026