Identity
- Trade Name
- AURORA® FDA UDI
- Generic Name
- Endoscopic video image processing unit FDA UDI
- Device Name
- Surgiscope® System Power Cable FDA UDI
- Model / Reference
- ICB/PC FDA UDI
- Description
- Surgiscope® System Power Cable FDA UDI
Identifiers
- Catalog Number
- ICB/PC FDA UDI
- Primary DI / UDI-DI
- 00850002332049 FDA UDI
- 510(k) Number
- K201840 FDA UDI
- FDA Product Code
- GWG FDA UDIGZT FDA UDI
- GMDN Term
- Endoscopic video image processing unit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1480 FDA UDI882.4800 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Endoscopic video image processing unit
Aurora® by Rebound Therapeutics, Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscopic video image processing unit.
- Pixa — SANTA BARBARA IMAGING SYSTEMS, INC. · Class II
- ILO — ILO electronic GmbH · Class I
- AURORA® Surgiscope® — Integra Lifesciences Corp. · Class II
- VIDEO PROCESSOR — PENTAX of America, Inc. · Class II
- Digital Video Processor — Hunan Vathin Medical Instrument Co., Ltd · Class II
- ILO — ILO electronic GmbH · Class I
- 3NT Video Console — 3nt Medical , Ltd. · Class II
- HDMI cable — MacroLux Medical Technology Co., Ltd. · 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
- Rebound Therapeutics, Corporation
Sources (1)
- FDA UDI 73384541-c767-4519-8f93-c65313f54890 37 fields · synced May 29, 2026