Primary Device ID | 08720648846083 |
NIH Device Record Key | 4466f592-035f-42a8-89b1-f0093df6e1ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flowsensor3-BT |
Version Model Number | Flowsensor3-BTLE |
Company DUNS | 416277333 |
Company Name | Medical Measurement Systems B.V. |
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 | 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 | 08720648846083 [Primary] |
EXQ | Cystometer, Electrical Recording |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-25 |
Device Publish Date | 2024-09-17 |
08720648846083 - Flowsensor3-BT | 2024-09-25 |
08720648846083 - Flowsensor3-BT | 2024-09-25 |
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08717775955870 - HEM FS | 2022-11-28 |
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