Aed 32-4220
by National Advanced Endoscopy Devices, Inc. 2 variants
Aed 32-4220 is a Class II device made by National Advanced Endoscopy Devices, Inc., listed in FDA GUDID since 7 May 2019 (UDI-DI 00848657016360), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00848657016360 | Date7 May 2019 | StatusListed |
Official records
- AccessGUDID record 00848657016360
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aed
- Generic name
- Resectoscope
- Model / reference
- 32-4220
- Primary DI / UDI-DI
- 00848657016360
- FDA product code
- FDC
- GMDN term
- Resectoscope
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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