Primary Device ID | 00382904905231 |
NIH Device Record Key | 0bb453fa-580c-4150-a16f-ac189b1fbc8b |
Commercial Distribution Discontinuation | 2015-08-26 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | BD PrepStain |
Version Model Number | 490523 |
Catalog Number | 490523 |
Company DUNS | 103318015 |
Company Name | TRIPATH IMAGING, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-800-638-8663 |
technical_services@bd.com | |
Phone | 1-800-638-8663 |
technical_services@bd.com |
Length | 59.4 Centimeter |
Length | 59.4 Centimeter |
Length | 59.4 Centimeter |
Height | 43.5 Centimeter |
Width | 34.5 Centimeter |
Length | 59.4 Centimeter |
Storage Environment Temperature | Between 15 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 15 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382904905231 [Primary] |
MKQ | Processor, Cervical Cytology Slide, Automated |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-07-22 |
00382904905286 | PrepStain® Install Kit |
00382904905231 | PrepStain® GYN Cytology Test Kit |
00382904905217 | PrepStain® Density Reagent |