NexPak 9110524
NexPak 9110524 is a Class I device made by Hemostasis, LLC, listed in FDA GUDID since 30 Sep 2020 (UDI-DI 00858439001613), registry data as of 22 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 | Number00858439001613 | Date30 Sep 2020 | StatusListed |
Official records
- AccessGUDID record 00858439001613
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- NexPak
- Generic name
- Intranasal splint, non-biodegradable
- Model / reference
- 9110524
- Primary DI / UDI-DI
- 00858439001613
- FDA product code
- LYA
- GMDN term
- Intranasal splint, non-biodegradable
- Device class
- Class I
- Regulation number
- 874.4780
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 0.5 InchLength — 1.75 Inch
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