Primary Device ID | 07612367038652 |
NIH Device Record Key | 8b5fe1d2-20cc-410f-89b9-3c068385c129 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Thopaz disposable canister 0.3l |
Version Model Number | 079.0011 |
Company DUNS | 488293218 |
Company Name | Medela AG |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07612367013758 [Primary] |
GS1 | 07612367038652 [Package] Contains: 07612367013758 Package: [24 Units] Discontinued: 2017-07-14 Not in Commercial Distribution |
GS1 | 07612367063357 [Package] Contains: 07612367013758 Package: [12 Units] In Commercial Distribution |
BTA | Pump, Portable, Aspiration (Manual Or Powered) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 7 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2017-06-07 |
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