Identity
- Trade Name
- Visionflex FDA UDI
- Generic Name
- Surgical camera lens FDA UDI
- Device Name
- GEIS Camera (General Examination Imaging System) is a handheld device that can capture medical grade quality images and video in Full HD 1080p resolution at the touch of a button. FDA UDI
- Model / Reference
- VFGEISCAM1.04 FDA UDI
- Description
- GEIS Camera (General Examination Imaging System) is a handheld device that can capture medical grade quality images and video in Full HD 1080p resolution at the touch of a button. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 09352527000775 FDA UDI
- FDA Product Code
- FWB FDA UDI
- GMDN Term
- Surgical camera lens FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4160 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
No
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical camera lens
Visionflex by Visionflex Pty. Ltd. — 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
- Visionflex Pty. Ltd.
Sources (1)
- FDA UDI 97682cfd-31d8-4b59-9add-3d883d11cc5f 33 fields · synced May 30, 2026