Primary Device ID | 07612367064668 |
NIH Device Record Key | 786e68cc-cb7f-4b3f-99e9-1e6037e39136 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Diposable Overflow Protection / Virus filter |
Version Model Number | 101035263 |
Company DUNS | 488293218 |
Company Name | Medela AG |
Device Count | 10 |
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 | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1-877-735-1626 |
info-healthcare@medela.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07612367064651 [Primary] |
GS1 | 07612367064668 [Package] Contains: 07612367064651 Package: [20 Units] In Commercial Distribution |
GS1 | 07612367064675 [Unit of Use] |
BTA | Pump, Portable, Aspiration (Manual Or Powered) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-08 |
Device Publish Date | 2019-04-30 |
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