| Primary Device ID | 00197998470523 |
| NIH Device Record Key | 61db97f8-a1b5-4861-8211-a840973ad0e0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Littmann® Classic III™ |
| Version Model Number | 5623C |
| Catalog Number | 5623C |
| Company DUNS | 119004140 |
| Company Name | Solventum US LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| OTC Over-The-Counter | true |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com | |
| Phone | +1(800)634-2249 |
| regulatoryrequests@solventum.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00197998470516 [Primary] |
| GS1 | 00197998470523 [Package] Contains: 00197998470516 Package: [1 Units] In Commercial Distribution |
| LDE | STETHOSCOPE, MANUAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-02-11 |
| Device Publish Date | 2026-02-03 |
| 00197998470523 | Littmann® Classic III™ Stethoscope, 5623C, Stainless-finishChestpiece, Satin-finish Caribbean |
| 00197998470509 | Littmann® Classic III™ Stethoscope, 5648C, Stainless-finishChestpiece, Satin-finish Raspberry |
| 00197998470486 | Littmann® Classic III™ Stethoscope, 5620C, Stainless-finishChestpiece, Satin-finish Black Tub |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LITTMANN 97096152 not registered Live/Pending |
3M Company 2021-10-27 |
![]() LITTMANN 88801580 not registered Live/Pending |
3M Company 2020-02-18 |
![]() LITTMANN 88794112 not registered Live/Pending |
3M Company 2020-02-12 |
![]() LITTMANN 88749841 not registered Live/Pending |
3M Company 2020-01-07 |
![]() LITTMANN 85968847 4477862 Live/Registered |
3M Company 2013-06-25 |
![]() LITTMANN 78118227 2683822 Live/Registered |
3M COMPANY 2002-03-28 |
![]() LITTMANN 73403537 1276855 Dead/Cancelled |
Minnesota Mining and Manufacturing Company 1982-11-22 |
![]() LITTMANN 73143618 1115217 Live/Registered |
MINNESOTA MINING AND MANUFACTURING COMPANY 1977-10-04 |
![]() LITTMANN 73051964 1040890 Dead/Expired |
MINNESOTA MINING AND MANUFACTURING COMPANY 1975-05-09 |
![]() LITTMANN 73030702 1034725 Dead/Expired |
MINNESOTA MINING AND MANUFACTURINGCOMPANY 1974-08-29 |
![]() LITTMANN 72461110 0998220 Dead/Expired |
MINNESOTA MINING AND MANUFACTURINGCOMPANY 1973-06-22 |
![]() LITTMANN 72427694 0988946 Dead/Expired |
MINNESOTA MINING AND MANUFACTURING COMPANY 1972-06-19 |