ImageMax 950
by Tate Technology, Inc. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00862879000303 | Date1 Nov 2016 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- Trade Name
- ImageMax
- Generic Name
- Dental automated x-ray film processor
- Model / Reference
- 950
- Primary DI / UDI-DI
- 00862879000303
- FDA Product Code
- EGY
- GMDN Term
- Dental automated x-ray film processor
- Device Class
- Class II
- Regulation Number
- 892.1900
- Commercial Distribution
- Not in Commercial Distribution
Properties
Other properties (13)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
- Manufacturing Date: No