Primary Device ID | 30884838014542 |
NIH Device Record Key | b7c15cf3-cefe-4d24-a860-7bd3fbee0148 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 989803164921 |
Catalog Number | 989803164921 |
Company DUNS | 314101143 |
Company Name | Philips Medizin Systeme Böblingen GmbH |
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 | true |
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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Phone | +1(999)999-9999 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 30884838014542 [Primary] |
DQA | Oximeter |
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 | 2016-11-22 |
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