Jedmed 53-2487
Jedmed 53-2487 is a Class I device made by JEDMED Instrument Company, listed in FDA GUDID since 19 Jan 2023 (UDI-DI M6335324870), 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 | NumberM6335324870 | Date19 Jan 2023 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Jedmed
- Generic name
- Paranasal sinus irrigation/aspiration cannula
- Model / Ref / Catalog
- 53-2487
- Primary DI / UDI-DI
- M6335324870
- FDA product code
- KAM
- GMDN term
- Paranasal sinus irrigation/aspiration cannula
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code KAM (Cannula, Sinus).
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- Suction tube 20-570-18 by Spiggle & Theis Medizintechnik GmbH
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- RAINS FRONTAL SINUS STENT by Smith & Nephew Richards, Inc.
- SINOJECT MAXILLARY SINUS PUNCTURE & IRRIGATION SYS by Atos Medical AB
- SINOJET MAXILLARY SINUS PUNCTURE & IRRIGATION SYSTEM by Atos Medical AB
- RELIEVA LUMA SINUS ILLUMINATION SYSTEM, MODEL SIS-100A by ACCLARENT, INC.
- RELIEVA STRATUS MICROFLOW SPACER by ACCLARENT, INC.
- FRONTAL SINUS TREPHINATION CANNULA by Xomed, Inc.
- SHIKANI MIDDLE MEATAL ANTROSTOMY VENT TUBE by Micromedics, Inc.