Identity
- Trade Name
- Artemis FDA UDI
- Generic Name
- Surgical irrigation/aspiration system FDA UDI
- Device Name
- Artemis 2.8 mm FDA UDI
- Model / Reference
- AP28-A FDA UDI
- Description
- Artemis 2.8 mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00814548017877 FDA UDI
- 510(k) Number
- K171332 FDA UDI
- FDA Product Code
- GWG FDA UDI
- GMDN Term
- Surgical irrigation/aspiration system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1480 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical irrigation/aspiration system
Artemis by Penumbra, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical irrigation/aspiration system.
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- ZOOM Aspiration Pump — Taiwan Biomaterial Co., Ltd. · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- LMI IRRIGATION (STRAIGHT) CATHETER — LUCAS MEDICAL INC · Class II
- LMI IRRIGATION (STRAIGHT) CATHETER — LUCAS MEDICAL INC · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
- ROCAFLOW Irrigation, Warming and Suction System — Promepla · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class II
Cleared under the same submission
K171332 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
- Penumbra, Inc.
Sources (1)
- FDA UDI 7c1ad7b5-4760-4a82-a645-f679e4ef6164 34 fields · synced May 30, 2026