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Filter Sampler Blood Serum Filter

FDA UDI

Class II (US FDA UDI)

by Porex Corporation

Identity

Trade Name
Filter Sampler Blood Serum Filter FDA UDI
Generic Name
Evacuated blood collection tube IVD, no additive/metal-free FDA UDI
Device Name
16mm x 4" Filter Sampler Blood Serum Filter IB Model FDA UDI
Model / Reference
IB Model FDA UDI
Description
16mm x 4" Filter Sampler Blood Serum Filter IB Model FDA UDI

Identifiers

Catalog Number
6251 FDA UDI
Primary DI / UDI-DI
10817139020116 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

No

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 Blood Serum 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 21566031-0bb4-4ec4-b91f-321d322c6c2f 36 fields · synced May 30, 2026