AbbVie NJ 62903
by Abbvie Inc.
AbbVie NJ 62903 is a Class II device made by Abbvie Inc., listed in FDA GUDID since 15 Apr 2019 (UDI-DI 38054083008302), 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 | Number38054083008302 | Date15 Apr 2019 | StatusListed |
Official records
- AccessGUDID record 38054083008302
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- AbbVie NJ
- Generic name
- Nasoenteral tube
- Model / reference
- 62903
- Primary DI / UDI-DI
- 38054083008302
- FDA product code
- KNT
- GMDN term
- Nasoenteral tube
- Device class
- Class II
- Regulation number
- 876.5980
- GUDID distribution status
- In Commercial Distribution
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