Primary Device ID | 20884838008629 |
NIH Device Record Key | 4f380ad2-e347-4043-b310-d6220f8d61bc |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 989803106021 |
Catalog Number | 989803106021 |
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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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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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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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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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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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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Phone | +1(999)999-9999 |
xx@xx.xx |
Storage Environment Temperature | Between 0 Degrees Celsius and 60 Degrees Celsius |
Storage Environment Temperature | Between 32 Degrees Fahrenheit and 140 Degrees Fahrenheit |
Storage Environment Humidity | Between 5 Percent (%) Relative Humidity and 80 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838008625 [Unit of Use] |
GS1 | 20884838008629 [Primary] |
HGM | SYSTEM, MONITORING, PERINATAL |
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 | 2017-03-03 |