Mdp
Mdp (302-10005) is a Class I device made by Quality Aspirators, listed in FDA GUDID since 27 Feb 2025 (UDI-DI 00814005023380), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00814005023380 | Date27 Feb 2025 | StatusListed |
Official records
- AccessGUDID record 00814005023380
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- General-purpose light source
- Model / Ref / Catalog
- MDP, 302-10005
- Primary DI / UDI-DI
- 00814005023380
- FDA product code
- EAY
- GMDN term
- General-purpose light source
- Device class
- Class I
- Regulation number
- 872.4620
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices
Other devices filed under FDA product code EAY (LIGHT, FIBER OPTIC, DENTAL).
- FIBER OPTIC LIGHT SOURCE I by Venture Technology, Inc.
- DENTISCOPE by Chayes Virginia, Inc.
- FIBER OPTIC ILLUMINATOR by Lares Manufacturing Co., Inc.
- ORALUMINATOR III - LIGHT SOURCE FOR F.O. by Midwest
- POWER OPTIC by Ritter Co.
- JEDENTAL VLC DENTAL CURING LIGHT by Jedental Co., Inc.
- ORALUMINATOR III AUTO-LIGHT by Midwest
- DEN-MAT FIBER OPTIC HALOGEN LIGHT by Den-Mat Corp.
- OPUS I OPTION - FIBER OPTIC L SYSTEM by Syntex Corp.
- FIBER OPTIC HOSE by Lares Manufacturing Co., Inc.