Identity
- Trade Name
- HMS PLUS FDA UDI
- Generic Name
- Coagulation timer IVD FDA UDI
- Device Name
- RESERVOIR 31506 HMS FDA UDI
- Model / Reference
- 31506 FDA UDI
- Description
- RESERVOIR 31506 HMS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00721902433719 FDA UDI
- 510(k) Number
- K894317 FDA UDI
- FDA Product Code
- JOX FDA UDI
- GMDN Term
- Coagulation timer IVD FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.5680 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
No
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: Coagulation timer IVD
Hms Plus by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coagulation timer IVD.
- ACT Plus® — MEDTRONIC, INC. · Class II
- ACT Plus® — MEDTRONIC, INC. · Class II
- ACT Plus® — MEDTRONIC, INC. · Class II
- HMS PLUS — MEDTRONIC, INC. · Class II
- ACT Plus® — MEDTRONIC, INC. · Class II
- ACT Plus® — MEDTRONIC, INC. · Class II
- HMS PLUS — MEDTRONIC, INC. · Class II
- HEPtrac® — MEDTRONIC, INC. · Class II
Cleared under the same submission
K894317 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI b618667e-944e-415b-a927-25ad74d9a0d5 35 fields · synced May 30, 2026