Imaging Plate
by Carestream Health, Inc. 14 variants
Imaging Plate (1098912) is a Class I device made by Carestream Health, Inc., listed in FDA GUDID since 16 Sep 2016 (UDI-DI 40889971098913), registry data as of 8 Jun 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number40889971098913 | Date16 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 40889971098913
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Digital imaging storage phosphor screen
- Model / Ref / Catalog
- Imaging Plate, 1098912
- Primary DI / UDI-DI
- 40889971098913
- FDA product code
- EAM
- GMDN term
- Digital imaging storage phosphor screen
- Device class
- Class I
- Regulation number
- 892.1960
- GUDID distribution status
- In Commercial Distribution
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- FUJI IMAGING PLATE IP HR-BD 18X24CM 2 E 47410-05942 by FUJIFILM CORPORATION
- RADIOGRAPHIC INTENSIFYING SCREEN by INFAB, LLC.
- FUJI UM MAMMO SERIES INTENSIFY SCREENS: by Fujifilm Medical System U.S.A., Inc.