Identity
- Trade Name
- Uscope FDA UDI
- Generic Name
- Flexible video ureteroscope, single-use FDA UDI
- Device Name
- This instrument has been designed to be used with Endo-Therapy accessories such as a biopsy forceps and other ancillary equipment for endoscopy and endoscopic surgery within urinary tract and interior of the kidney. This instrument is also used as a suction catheter that establishes a conduit used for irrigation and aspiration of kidney stones and stone dust during ureteral lithotripsy. This instrument is labeled Reverse Deflection. FDA UDI
- Model / Reference
- PU411A (Reverse Deflection) FDA UDI
- Description
- This instrument has been designed to be used with Endo-Therapy accessories such as a biopsy forceps and other ancillary equipment for endoscopy and endoscopic surgery within urinary tract and interior of the kidney. This instrument is also used as a suction catheter that establishes a conduit used for irrigation and aspiration of kidney stones and stone dust during ureteral lithotripsy. This instrument is labeled Reverse Deflection. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06971176281309 FDA UDI
- 510(k) Number
- K233778 FDA UDI
- FDA Product Code
- FGB FDA UDIFED FDA UDI
- GMDN Term
- Flexible video ureteroscope, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Flexible video ureteroscope, single-use
Uscope by Zhuhai Pusen Medical Technology Co, Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible video ureteroscope, single-use.
- Single-use Flexible Uretero-Renoscope — Zhuhai Vision Medical Technology Co., Ltd · Class IIa
- Ureterorenoscope — Innoview GmbH · Class IIa
- WiScope® — OTU MEDICAL INC. · Class II
- URS. 040.00.1500 — Blazejewski MEDI-TECH GmbH · Class IIa
- CoralView® — MacroLux Medical Technology Co., Ltd. · Class II
- LithoVue — Boston Scientific · Class II
- Single-use Digital Flexible Ureterorenoscopes — NINGBO XINWELL MEDICAL TECHNOLOGY CO., LTD. · Class IIa
- Flexible Ureterorenoscopes — Shanghai Anqing Medical Instrument Co., Ltd · Class IIa
Cleared under the same submission
K233778 also covers:
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
- Uscope — Zhuhai Pusen Medical Technology Co, Ltd
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 |
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Manufacturer
- Manufacturer
- Zhuhai Pusen Medical Technology Co, Ltd
Sources (1)
- FDA UDI 7a79fcb4-fc1b-4245-8652-7ba1b4aaa513 34 fields · synced Jun 6, 2026