Jedmed 52-2182
Jedmed 52-2182 is an ear speculum (FDA Class I; FDA product code EPY, Speculum, Ent) made by JEDMED Instrument Company, listed in FDA GUDID since 21 Sep 2020 (UDI-DI M6335221820), 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 | NumberM6335221820 | Date21 Sep 2020 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Jedmed
- Generic name
- Ear speculum, single-use
- Model / Ref / Catalog
- 52-2182
- Primary DI / UDI-DI
- M6335221820
- FDA product code
- EPY
- GMDN term
- Ear speculum, single-use
- Device class
- Class I
- Regulation number
- 878.1800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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