OrthoGrid® 20-8025-210-00
by Orthogrid Systems, Inc United States GUDID
Product code LHO
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00889024707450 | Date15 Jul 2026 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- OrthoGrid®
- Generic Name
- Radiographic test pattern
- Model / Reference
- 20-8025-210-00
- Primary DI / UDI-DI
- 00889024707450
- FDA Product Code
- LHO
- GMDN Term
- Radiographic test pattern
- Device Class
- Class I
- Regulation Number
- 892.1940
- Commercial Distribution
- In Commercial Distribution
- Size
- Outer Diameter — 12 Inch
Other devices from Orthogrid Systems, Inc
Properties & raw data
Show properties, registry sources and raw records
Other properties (8)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Expiration Date: No
Sources (1)
- FDA UDI 74aeddca-2e30-423f-8352-79d4416c88d4