V-Ject DN14I-2738
V-Ject DN14I-2738 is a Class I device made by Vericom Co., Ltd., listed in FDA GUDID since 25 Jun 2025 (UDI-DI 08800123814865), 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 | Number08800123814865 | Date25 Jun 2025 | StatusListed |
Official records
- AccessGUDID record 08800123814865
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- V-Ject
- Generic name
- Dental syringe needle, single-use
- Model / reference
- DN14I-2738
- Primary DI / UDI-DI
- 08800123814865
- FDA product code
- DZM
- GMDN term
- Dental syringe needle, single-use
- Device class
- Class I
- Regulation number
- 872.4730
- GUDID distribution status
- In Commercial Distribution
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