Aed 32-4221RR
by National Advanced Endoscopy Devices, Inc.
Aed 32-4221RR is a Class II device made by National Advanced Endoscopy Devices, Inc., listed in FDA GUDID since 30 Jun 2017 (UDI-DI 00848657015462), 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 | Number00848657015462 | Date30 Jun 2017 | StatusListed |
Official records
- AccessGUDID record 00848657015462
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aed
- Generic name
- Resectoscope
- Model / reference
- 32-4221RR
- Primary DI / UDI-DI
- 00848657015462
- FDA product code
- FJL
- GMDN term
- Resectoscope
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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