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PALL® PharmAssure 25 mm HYDROPHOBIC VENT FILTER

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref HP2002

by Pall International SARL

Identity

Trade Name
PALL® PharmAssure 25 mm HYDROPHOBIC VENT FILTER EUDAMED
Pall PharmAssure® 25 mm Hydrophobic Vent Filter FDA UDI
Generic Name
Hydrophobic Luer filter, sterile FDA UDI
Device Name
Pall PharmAssure 25mm Hydrophobic Vent Filter EUDAMED
25 mm 0.2 micron hydrophobic vent filter FDA UDI
Model / Reference
HP2002 EUDAMEDFDA UDI
Description
25 mm 0.2 micron hydrophobic vent filter FDA UDI

Identifiers

Catalog Number
HP2002 FDA UDI
Primary DI / UDI-DI
05034480310125 EUDAMEDFDA UDI
Basic UDI-DI
5034480VNTF05NINVW6 EUDAMED
FDA Product Code
FMF FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Hydrophobic Luer filter, sterile FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
Market of Registration
Belgium 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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Pore Size — 0.2 Micrometer FDA UDI

Category: Device sterilization/disinfection container, reusable

PALL® PharmAssure 25 mm HYDROPHOBIC VENT FILTER by Pall International SARL — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CH-MF-000023177
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (2)

  • EUDAMED 2970f545-5f6e-467f-a4b9-1ae122eebdfc 61 fields · synced Jul 11, 2026
  • FDA UDI 3baff37c-19fb-4056-b4db-1bab1c5f7b24 36 fields · synced May 30, 2026