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Fisherbrand Serum Filter

FDA UDI

Class II (US FDA UDI)

by Porex Corporation

Identity

Trade Name
Fisherbrand Serum Filter FDA UDI
Generic Name
Evacuated blood collection tube IVD, no additive/metal-free FDA UDI
Device Name
16mm x 1 7/8" Fisherbrand Serum Filter Standard Model FDA UDI
Model / Reference
Standard Model FDA UDI
Description
16mm x 1 7/8" Fisherbrand Serum Filter Standard Model FDA UDI

Identifiers

Catalog Number
02-681-61 FDA UDI
Primary DI / UDI-DI
10817139020543 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

Fisherbrand 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 910246e9-1f69-473d-8a12-3902ba1fa471 35 fields · synced May 30, 2026