Primary Device ID | B1603002C1 |
NIH Device Record Key | 5fc4a93e-2692-4d21-a875-3b92cbc1a771 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Procedure Products Medicine Cup |
Version Model Number | 3002-C |
Catalog Number | 3002-C |
Company DUNS | 151507563 |
Company Name | PROCEDURE PRODUCTS, 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B1603002C1 [Primary] |
KYW | Container, Liquid Medication, Graduated |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2018-02-12 |
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