Identity
- Trade Name
- LUCAS FDA UDI
- Generic Name
- Cardiac resuscitator, line-powered FDA UDI
- Device Name
- LUCAS 3, 3.1, IN SHIPPING BOX, EN FDA UDI
- Model / Reference
- 99576 FDA UDI
- Description
- LUCAS 3, 3.1, IN SHIPPING BOX, EN FDA UDI
Identifiers
- Catalog Number
- 99576-000063 FDA UDI
- Primary DI / UDI-DI
- 00883873834329 FDA UDI
- FDA Product Code
- DRM FDA UDI
- GMDN Term
- Cardiac resuscitator, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5200 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
Yes
FDA UDI
Category: Cardiac resuscitator, line-powered
Lucas by Jolife AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiac resuscitator, line-powered.
- AutoPulse®Resuscitation System — ZOLL Circulation, Inc. · Class II
- AutoPulse®Resuscitation System — ZOLL Circulation, Inc. · Class II
- AutoPulse®Resuscitation System — ZOLL Circulation, Inc. · Class II
- AutoPulse®Resuscitation System — ZOLL Circulation, Inc. · Class II
- AutoPulse®Resuscitation System — ZOLL Circulation, Inc. · Class II
- AutoPulse®Resuscitation System — ZOLL Circulation, Inc. · Class II
- Defibtech ACC Configuration — DEFIBTECH, L.L.C. · Class II
- AutoPulse®Resuscitation System — ZOLL Circulation, Inc. · Class II
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
- Jolife AB
Sources (1)
- FDA UDI b747f876-7765-42a1-aeb5-fe97d6c3717e 35 fields · synced May 30, 2026