Identity
- Trade Name
- MiniMed™ Quick-serter™ FDA UDI
- Generic Name
- Injector reset device FDA UDI
- Device Name
- SERTER MMT-305QS QCKSRTR QCKST 23L FDA UDI
- Model / Reference
- MMT-305QS FDA UDI
- Description
- SERTER MMT-305QS QCKSRTR QCKST 23L FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00643169698116 FDA UDI
- 510(k) Number
- K160860 FDA UDI
- FDA Product Code
- KZH FDA UDI
- GMDN Term
- Injector reset device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6920 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
No
FDA UDI
Category: Injector reset device
MiniMed™ Quick-serter™ by Medtronic Minimed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K160860 also covers:
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
- Medtronic Minimed, Inc.
Sources (1)
- FDA UDI 852206f2-61a7-4e3d-a284-aab87574bd44 35 fields · synced Jun 1, 2026