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903™

FDA UDIEUDAMED

Class II (US FDA UDI)

by Eastern Business Forms, LLC

Identity

Trade Name
903™ FDA UDI
Generic Name
Blood collection paper FDA UDI
Device Name
903 Filter Paper Lot#-variable FDA UDI
Model / Reference
Variable FDA UDI
Description
903 Filter Paper Lot#-variable FDA UDI

Identifiers

Primary DI / UDI-DI
00850039198014 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Blood collection paper 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood collection paper

903™ by Eastern Business Forms, LLC — Class II — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Blood collection paper.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 305d29bb-4f8f-4bb3-a094-743615593777 33 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026