Identity
- Trade Name
- Lucas PCI Back Plate FDA UDI
- Generic Name
- Cardiac compression board FDA UDI
- Device Name
- LUCAS PCI BACK PLATE FDA UDI
- Model / Reference
- 11576 FDA UDI
- Description
- LUCAS PCI BACK PLATE FDA UDI
Identifiers
- Catalog Number
- 11576-000064 FDA UDI
- Primary DI / UDI-DI
- 00883873948286 FDA UDI
- 510(k) Number
- K090422 FDA UDI
- FDA Product Code
- DRM FDA UDI
- GMDN Term
- Cardiac compression board 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Cardiac compression board
Lucas PCI Back Plate by Jolife AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiac compression board.
- HUDSON RCI — TELEFLEX INCORPORATED · Class I
- Spencer — SPENCER ITALIA SRL · Class I
- HUDSON RCI — TELEFLEX INCORPORATED · Class I
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 097bcc7a-a20b-4399-90a1-8a93319d00e7 36 fields · synced May 30, 2026