Primary Device ID | 00858293006069 |
NIH Device Record Key | f20ed384-80da-4765-b956-25e1102b2589 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RPC |
Version Model Number | 480007-CC |
Catalog Number | 480007-CC |
Company DUNS | 796083392 |
Company Name | REPROCESSING PRODUCTS CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00858293006069 [Primary] |
MSY | Strip, Test, Reagent, Residuals For Dialysate, Disinfectant |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-08-16 |
Device Publish Date | 2017-01-19 |
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00858293006069 | K100-0118 Color Card |
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