Identity
- Trade Name
- Littmann® Telesteth™ FDA UDI
- Generic Name
- Stethoscope application software FDA UDI
- Device Name
- TS1200CL TELESTETH SOFTWARE HOSTED LICENSE FDA UDI
- Model / Reference
- TS1200CL FDA UDI
- Description
- TS1200CL TELESTETH SOFTWARE HOSTED LICENSE FDA UDI
Identifiers
- Catalog Number
- TS1200CL FDA UDI
- Primary DI / UDI-DI
- 00707387766597 FDA UDI
- 510(k) Number
- K120704 FDA UDI
- FDA Product Code
- DRG FDA UDI
- GMDN Term
- Stethoscope application software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2910 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Stethoscope application software
Littmann® Telesteth™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Stethoscope application software.
- ClearSteth — GlobalMed Holdings, LLC · Class II
- Stethee Pro Mobile Android Application — M3Dicine Pty , Ltd. · Class I
- Stethee Pro Central Web Application — M3Dicine Pty , Ltd. · Class I
- Stethee Pro Mobile iOS Application — M3Dicine Pty , Ltd. · Class I
- 3M™ Littmann® — 3M COMPANY · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- 3m Company
Sources (1)
- FDA UDI e185c37a-0bf0-4ae4-9155-6080807a391e 36 fields · synced May 30, 2026