Pilling IPN006405
Pilling IPN006405 (380210) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 24026704525632), 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 | Number24026704525632 | Date15 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 24026704525632
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pilling
- Generic name
- Brain spatula
- Model / Ref / Catalog
- IPN006405, 380210
- Primary DI / UDI-DI
- 24026704525632
- FDA product code
- HAO
- GMDN term
- Brain spatula
- Device class
- Class I
- Regulation number
- 882.4535
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Width — 25 MillimeterLength — 18 Centimeter
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