Primary Device ID | 10860802000380 |
NIH Device Record Key | bc16b8f6-4bb0-4c4b-949e-fee6b929b32d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 903™ |
Version Model Number | W201 |
Company DUNS | 079861573 |
Company Name | EASTERN BUSINESS FORMS INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860802000383 [Primary] |
GS1 | 10860802000380 [Package] Contains: 00860802000383 Package: [10000 Units] In Commercial Distribution |
JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-11 |
Device Publish Date | 2021-03-03 |
10860802000366 | 903 Filter Paper |
00860802000352 | 903 Filter Paper |
10860802000342 | 903 Filter Paper |
00860802000338 | 903 Filter Paper |
10860802000373 | 903 Filter Paper |
10860802000380 | 903 Filter Paper |
00850039198014 | 903 Filter Paper Lot#-variable |
00850039198007 | 903 Filter Paper |
10850039198028 | W221 |
10850039198042 | W231 |