Identity
- Trade Name
- QuantStudio Dx Software V1.0.3, Kit FDA UDI
- Generic Name
- Laboratory instrument/analyser application software IVD FDA UDI
- Device Name
- KIT,QS DX SW V1.0.3 FDA UDI
- Model / Reference
- 1.0.3 FDA UDI
- Description
- KIT,QS DX SW V1.0.3 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10190302006729 FDA UDI
- 510(k) Number
- K123955 FDA UDI
- FDA Product Code
- OOI FDA UDI
- GMDN Term
- Laboratory instrument/analyser application software IVD FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.2570 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Laboratory instrument/analyser application software IVD
QuantStudio Dx Software V1.0.3, Kit by Life Technologies Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K123955 also covers:
- Fast 96-Well Block — LIFE TECHNOLOGIES HOLDINGS PTE. LTD.
- Fast 96-Well Heater Cover — LIFE TECHNOLOGIES HOLDINGS PTE. LTD.
- Lamp, Halogen RC, IVD — LIFE TECHNOLOGIES HOLDINGS PTE. LTD.
- QuantStudio(TM) Dx Software Version 1.0.4 — LIFE TECHNOLOGIES HOLDINGS PTE. LTD.
- QuantStudioTM Dx Real-Time PCR Instrument — LIFE TECHNOLOGIES HOLDINGS PTE. LTD.
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
- Life Technologies Limited
Sources (1)
- FDA UDI 2395d344-bfe8-41fd-ab95-987e117c666b 34 fields · synced Jun 8, 2026