| Primary Device ID | 50707387792430 |
| NIH Device Record Key | 620dc003-0313-4677-a196-5787851f12e4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 3M™ Littmann™ |
| Version Model Number | 8493 |
| Catalog Number | 8493 |
| Company DUNS | 830016148 |
| Company Name | 3M COMPANY |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00707387792435 [Primary] |
| GS1 | 50707387792430 [Package] Contains: 00707387792435 Package: BOX [3 Units] In Commercial Distribution |
| DQD | STETHOSCOPE, ELECTRONIC |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-08-07 |
| Device Publish Date | 2022-12-08 |
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