Pello 6290100000
Pello 6290100000 (6290-100-000) is a Class II device made by Stryker Corp., listed in FDA GUDID since 13 Sep 2023 (UDI-DI 07613327524116), 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 | Number07613327524116 | Date13 Sep 2023 | StatusListed |
Official records
- AccessGUDID record 07613327524116
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pello
- Generic name
- ENT shaver system handpiece
- Model / Ref / Catalog
- 6290100000, 6290-100-000
- Primary DI / UDI-DI
- 07613327524116
- FDA product code
- ERL
- GMDN term
- ENT shaver system handpiece
- Device class
- Class II
- Regulation number
- 874.4250
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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