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Filter Sampler Dispense Filter

FDA UDI

Class II (US FDA UDI)

by Porex Corporation

Identity

Trade Name
Filter Sampler Dispense Filter FDA UDI
Generic Name
Evacuated blood collection tube IVD, no additive/metal-free FDA UDI
Device Name
13mm x 4" Filter Sampler Dispense Filter Standard Model FDA UDI
Model / Reference
Standard Model FDA UDI
Description
13mm x 4" Filter Sampler Dispense Filter Standard Model FDA UDI

Identifiers

Catalog Number
6437 FDA UDI
Primary DI / UDI-DI
10817139020192 FDA UDI
FDA Product Code
GIM FDA UDI
GMDN Term
Evacuated blood collection tube IVD, no additive/metal-free FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Evacuated blood collection tube IVD, no additive/metal-free

Filter Sampler Dispense Filter by Porex Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Evacuated blood collection tube IVD, no additive/metal-free.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Porex Corporation

Sources (1)

  • FDA UDI 05137042-f916-459c-9921-d593e9aa73af 35 fields · synced May 30, 2026