NeoDevices, Inc. ND72DT
NeoDevices, Inc. ND72DT is a Class II device made by Neodevices Inc, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10816340022094), 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 | Number10816340022094 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 10816340022094
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- NeoDevices, Inc.
- Generic name
- Gastrostomy tube Y-piece connector
- Model / reference
- ND72DT
- Primary DI / UDI-DI
- 10816340022094
- FDA product code
- KNT
- GMDN term
- Gastrostomy tube Y-piece connector
- Device class
- Class II
- Regulation number
- 876.5980
- GUDID distribution status
- In Commercial Distribution
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