| Primary Device ID | 00020451904573 |
| NIH Device Record Key | 85d47674-5c5e-4bc8-af72-5003b65c9125 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Motion InBra™ |
| Version Model Number | 101047555 |
| Company DUNS | 052002029 |
| Company Name | Medela LLC |
| 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 | true |
| Manufacturing Date | true |
| 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 | true |
| Phone | 1-800-435-8316 |
| customer.service@medela.com | |
| Phone | 1-800-435-8316 |
| customer.service@medela.com | |
| Phone | 1-800-435-8316 |
| customer.service@medela.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00020451903880 [Primary] |
| GS1 | 00020451904573 [Package] Contains: 00020451903880 Package: [1 Units] In Commercial Distribution |
| GS1 | 00020451904764 [Direct Marking] |
| HGX | Pump, Breast, 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 | 2026-02-24 |
| Device Publish Date | 2026-02-16 |
| 00020451904573 | YM-8801 |
| 00020451904566 | YM-8801 |