Identity
- Trade Name
- Riptide™ FDA UDI
- Generic Name
- Surgical irrigation/aspiration pump, reusable FDA UDI
- Device Name
- PUMP MAP-1000 V02 NA RIPTIDE FDA UDI
- Model / Reference
- MAP-1000 FDA UDI
- Description
- PUMP MAP-1000 V02 NA RIPTIDE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000299415 FDA UDI
- 510(k) Number
- K172448 FDA UDI
- FDA Product Code
- NRY FDA UDI
- GMDN Term
- Surgical irrigation/aspiration pump, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1250 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical irrigation/aspiration pump, reusable
Riptide™ by Micro Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical irrigation/aspiration pump, reusable.
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- Tech Medical Services — TECH MEDICAL SERVICES, INC. · Class I
- CORE — Stryker Corp. · Class II
- ERBE — Erbe Elektromedizin GmbH · Class II
Cleared under the same submission
K172448 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
- Micro Therapeutics, Inc.
Sources (1)
- FDA UDI c8953e44-c81e-420b-bf2a-02c96d52247a 36 fields · synced Jun 1, 2026