Primary Device ID | 00884838008915 |
NIH Device Record Key | 28768c18-cd20-47e1-83e5-433d9eed4623 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 989803147961 |
Catalog Number | 989803147961 |
Company DUNS | 078628040 |
Company Name | Philips Medical Systems |
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 | 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 | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838008915 [Primary] |
OED | Antimicrobial blood pressure cuff |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2016-10-28 |