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Porges Coloplast

FDA UDI

Class I (US FDA UDI)

by Coloplast A/S

Identity

Trade Name
Porges Coloplast FDA UDI
Generic Name
Closed-wound/centesis drainage receptacle FDA UDI
Device Name
EASIVAC® / System for collecting pieces of tissue after TURP / Connector - ACMI FDA UDI
Model / Reference
E80403 FDA UDI
Description
EASIVAC® / System for collecting pieces of tissue after TURP / Connector - ACMI FDA UDI

Identifiers

Catalog Number
E80403 FDA UDI
Primary DI / UDI-DI
05705243322197 FDA UDI
FDA Product Code
FFD FDA UDI
GMDN Term
Closed-wound/centesis drainage receptacle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4370 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: Closed-wound/centesis drainage receptacle

Porges Coloplast by Coloplast A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound/centesis drainage receptacle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Coloplast A/S

Sources (1)

  • FDA UDI bbab0630-591d-4f37-adc5-7e78ef77f13a 36 fields · synced May 31, 2026