698344829
698344829 is a Class I device made by Depuy Spine, Inc., listed in FDA GUDID since 14 Nov 2023 (UDI-DI 10705034575018), 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 | Number10705034575018 | Date14 Nov 2023 | StatusListed |
Official records
- AccessGUDID record 10705034575018
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Drilling power tool attachment, basic
- Model / Ref / Catalog
- 698344829
- Primary DI / UDI-DI
- 10705034575018
- FDA product code
- HWE
- GMDN term
- Drilling power tool attachment, basic
- Device class
- Class I
- Regulation number
- 878.4820
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Drilling power tool attachment, basic.
- CHARLOTTE 41112017 by WRIGHT MEDICAL TECHNOLOGY, INC.
- Primado2 P200-2AS by NAKANISHI INC.
- ARS742000 by TORNIER, INC.
- Tornier Humeral Nail 7020140 by TORNIER, INC.
- P300-2S10 by NAKANISHI INC.
- RIGID MANDREL H0010050599 by HPF SRL
- ACUMED 45-0005-S by ACUMED LLC
- FLEX. MANDREL H0010050099 by HPF SRL
- 7207003000 by Stryker Corp.
- ACUMED 45-0023-S by ACUMED LLC