| 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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