Identity
- Trade Name
- Integra® Ruggles®-Redmond™ FDA UDI
- Generic Name
- Neurosurgical procedure kit, non-medicated, reusable FDA UDI
- Device Name
- Integra® Ruggles®-Redmond™ Bayonet Curette, Extra Large, Cervical, Set of 24 Instruments and 2 Trays FDA UDI
- Model / Reference
- RR8200 FDA UDI
- Description
- Integra® Ruggles®-Redmond™ Bayonet Curette, Extra Large, Cervical, Set of 24 Instruments and 2 Trays FDA UDI
Identifiers
- Catalog Number
- RR8200 FDA UDI
- Primary DI / UDI-DI
- 10381780234265 FDA UDI
- FDA Product Code
- OJH FDA UDIHAO FDA UDI
- GMDN Term
- Neurosurgical procedure kit, non-medicated, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI882.4535 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
Yes
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: General surgical procedure kit, non-medicated, reusableNeurosurgical procedure kit, non-medicated, reusable
Integra® Ruggles®-Redmond™ by Integra LifeSciences Production Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI 8da001d8-90dd-43bf-af2f-f825a7e6c491 35 fields · synced Jun 9, 2026