← Back to catalogue

Pall

FDA UDI

Class II (US FDA UDI)

by Pall International SARL

Identity

Trade Name
Pall FDA UDI
Generic Name
Haemodialysis system transducer protector FDA UDI
Device Name
Transducer Protector Hydrophobic Vent Filter (female and male slip luer) FDA UDI
Model / Reference
6254185 FDA UDI
Description
Transducer Protector Hydrophobic Vent Filter (female and male slip luer) FDA UDI

Identifiers

Catalog Number
6254185 FDA UDI
Primary DI / UDI-DI
05034480315106 FDA UDI
510(k) Number
K910821 FDA UDI
FDA Product Code
FIB FDA UDI
GMDN Term
Haemodialysis system transducer protector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Dimensions & Sizes

Size
Pore Size — 0.2 Micrometer FDA UDI

Category: Haemodialysis system transducer protector

Pall by Pall International SARL — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis system transducer protector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 5691c7df-882a-4948-a675-83b0604adadc 37 fields · synced May 30, 2026