FDA UDI Not in Commercial Distribution 🇺🇸 United States

AURORA Surgiscope

DI: 00860624000448 · Model: AURORA Surgiscope-13 · REBOUND THERAPEUTICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AURORA Surgiscope
Primary DI
00860624000448
Version / Model
AURORA Surgiscope-13
Catalog Number
AURORA Surgiscope-13
Company Name
REBOUND THERAPEUTICS CORPORATION
Labeler DUNS
080909607
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-22
Public Version
7
Public Version Date
2023-11-03
Public Version Status
Update
Public Device Record Key
ca060349-7e29-42cd-b20e-e4e54e08abeb
Distribution End Date
2019-11-24

Device Description

The AURORA Surgiscope System consists of two components: sterile, single use, neurological endoscope called the AURORA Surgiscope and a non-sterile, reusable control unit called the Image Control Box (ICB). The AURORA Surgiscope includes the following parts: Sheath, Camera, LEDs (Light Emitting Diodes), Sheath Cable, and Obturator.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GWG Endoscope, Neurological

GMDN Terms

Code Name
45045 Rigid optical intracranial/spinal endoscope, single-use

Identifiers

Type ID
Primary 00860624000448

Customer Contacts

Device Sizes

Type Value Unit Text
Length 13 Centimeter