Primary Device ID | 00816668020096 |
NIH Device Record Key | d8aef4af-388c-4d18-9bfa-557ad6145ac3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UNICO POWERSPIN BX |
Version Model Number | C885 |
Catalog Number | C885 |
Company DUNS | 796269165 |
Company Name | UNITED PRODUCTS & INSTRUMENTS |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | (732) 274-1155 |
info@unicosci.com | |
Phone | (732) 274-1155 |
info@unicosci.com | |
Phone | (732) 274-1155 |
info@unicosci.com | |
Phone | (732) 274-1155 |
info@unicosci.com | |
Phone | (732) 274-1155 |
info@unicosci.com | |
Phone | (732) 274-1155 |
info@unicosci.com | |
Phone | (732) 274-1155 |
info@unicosci.com | |
Phone | (732) 274-1155 |
info@unicosci.com | |
Phone | (732) 274-1155 |
info@unicosci.com | |
Phone | (732) 274-1155 |
info@unicosci.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816668020096 [Primary] |
GKG | Centrifuge, Hematocrit |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-04-10 |
00816668020102 | POWERSPIN™ BX CENTRIFUGE, VARIABLE SPEED 1,000-11,000 RPM, 8 PLACE AND 24PLACE MICROHEMATOCRIT |
00816668020096 | POWERSPIN™ BX CENTRIFUGE, VARIABLE SPEED 1,000-13,000 RPM WITH 8 PLACE TUBE ROTOR, 24 PLACE MI |
00816668020010 | C882 Microhematocrit Centrifuge, 24 place rotor, electronic timer. 110V |