Identity
- Trade Name
- MITEK CRUCIATE+ FDA UDI
- Generic Name
- Ligament reconstruction instrument set, reusable FDA UDI
- Device Name
- MITEK CRUCIATE+ ACL/PCL Femoral Point Aimer 2-40mm Plus or Minus 13 Percent FDA UDI
- Model / Reference
- 219008 FDA UDI
- Description
- MITEK CRUCIATE+ ACL/PCL Femoral Point Aimer 2-40mm Plus or Minus 13 Percent FDA UDI
Identifiers
- Catalog Number
- 219008 FDA UDI
- Primary DI / UDI-DI
- 10886705025763 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Ligament reconstruction instrument set, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ligament reconstruction instrument set, reusable
Mitek Cruciate+ by Medos International Sàrl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (2)
- FDA UDI 5ad7769b-0e31-4887-8447-e6d4487d0fa4 35 fields · synced Jun 19, 2026
- EUDAMED 1 fields · synced Jun 1, 2026