903™

GUDID 00850039198014

903 Filter Paper Lot#-variable

EASTERN BUSINESS FORMS INC

Blood collection paper
Primary Device ID00850039198014
NIH Device Record Key305d29bb-4f8f-4bb3-a094-743615593777
Commercial Distribution StatusIn Commercial Distribution
Brand Name903™
Version Model NumberVariable
Company DUNS079861573
Company NameEASTERN BUSINESS FORMS INC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100850039198014 [Primary]
GS110850039198011 [Package]
Package: [7200 Units]
In Commercial Distribution

FDA Product Code

JKATubes, Vials, Systems, Serum Separators, Blood Collection

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-02-07
Device Publish Date2022-01-28

On-Brand Devices [903™]

10860802000366903 Filter Paper
00860802000352903 Filter Paper
10860802000342903 Filter Paper
00860802000338903 Filter Paper
10860802000373903 Filter Paper
10860802000380903 Filter Paper
00850039198014903 Filter Paper Lot#-variable
00850039198007903 Filter Paper
10850039198028W221
10850039198042W231

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.