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KINCISE™ System Acetabular Cup Extraction Case Outlier Set
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- KINCISE™ System Acetabular Cup Extraction Case Outlier Set FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Model / Reference
- KIN-2110-07 FDA UDI
Identifiers
- Catalog Number
- 200005200 FDA UDI
- Primary DI / UDI-DI
- 08720828234198 FDA UDI
- FDA Product Code
- HWE FDA UDI
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Device sterilization/disinfection container, reusable
KINCISE™ System Acetabular Cup Extraction Case Outlier Set by Spierings Orthopaedics B.V. — Class I — FDA UDI — listed in FDA GUDID
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Spierings Orthopaedics B.V.
Sources (1)
- FDA UDI 36eb1117-0822-4740-b652-b009e7c4e614 33 fields · synced May 30, 2026