Primary Device ID | 07332834000486 |
NIH Device Record Key | a44ff614-7a80-425b-aeb2-f90f378e6821 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PROBE 407 Small Straight Probe |
Version Model Number | PROBE 407 |
Company DUNS | 354765570 |
Company Name | Perimed AB |
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 | false |
Serial Number | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07332834000486 [Primary] |
DPW | Flowmeter, Blood, Cardiovascular |
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 | 2016-09-13 |
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