Identity
- Trade Name
- MiniMed™ Reservoir FDA UDI
- Generic Name
- Ambulatory insulin infusion pump reservoir FDA UDI
- Device Name
- RSVR MMT-332A 10PK PRDGM 3ML 21L FDA UDI
- Model / Reference
- MMT-332A FDA UDI
- Description
- RSVR MMT-332A 10PK PRDGM 3ML 21L FDA UDI
Identifiers
- Primary DI / UDI-DI
- 70643169771481 FDA UDI
- 510(k) Number
- K032005 FDA UDI
- FDA Product Code
- OZP FDA UDIFRN FDA UDI
- GMDN Term
- Ambulatory insulin infusion pump reservoir FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 880.5725 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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: Ambulatory insulin infusion pump reservoir
MiniMed™ Reservoir by Medtronic Minimed, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Ambulatory insulin infusion pump reservoir.
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- Tandem Mobi Autosoft XC Kit — Tandem Diabetes Care, Inc. · Class II
Cleared under the same submission
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 III | Pending data |
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Manufacturer
- Manufacturer
- Medtronic Minimed, Inc.
Sources (1)
- FDA UDI 4dd52550-9036-489d-932a-8c392e3fd741 35 fields · synced May 30, 2026