Primary Device ID | 07612367017329 |
NIH Device Record Key | 68206f02-9e1c-416e-abf2-bc13e503c8ab |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Single set 1l, clampholder |
Version Model Number | 077.0701 |
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 | false |
Lot Batch | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07612367017329 [Primary] |
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 | 2024-06-10 |
Device Publish Date | 2024-05-31 |
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