Primary Device ID | 58052870818923 |
NIH Device Record Key | 3c1aa037-b843-4058-8cb4-3b79ed848d59 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | External Loader - Turn Table |
Version Model Number | W093-10 |
Catalog Number | W093-10 |
Company DUNS | 434263590 |
Company Name | COPAN WASP SRL |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +390302687218 |
wasp@copangroup.com | |
Phone | +390302687218 |
wasp@copangroup.com | |
Phone | +390302687218 |
wasp@copangroup.com | |
Phone | +390302687218 |
wasp@copangroup.com | |
Phone | +390302687218 |
wasp@copangroup.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 58052870818923 [Primary] |
JQW | Station, Pipetting And Diluting, For Clinical Use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-03 |
Device Publish Date | 2022-05-26 |
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58059796363964 - WASPLab® Double Incubator | 2024-06-12 WASPLab® Double Incubator |
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58052870817964 - Colibrí™ Primary Tube with Saline | 2024-02-08 Colibrí™ Primary Tube with Saline |
58059796361700 - URIVerse™ | 2023-10-30 URIVerse™ |
08050148218005 - Colibri Daily Verification Kit | 2022-11-23 Colibri Daily Verification Kit |