Spectrum, Inc. 985-03863-000
by Spectrum Co.
Spectrum, Inc. 985-03863-000 (712804LF) is a Class I device made by Spectrum Co., listed in FDA GUDID since 21 Jul 2017 (UDI-DI 00850301007778), registry data as of 22 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 | Number00850301007778 | Date21 Jul 2017 | StatusListed |
Official records
- AccessGUDID record 00850301007778
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Spectrum, Inc.
- Generic name
- Pressure bandage, non-latex, reusable
- Model / Ref / Catalog
- 985-03863-000, 712804LF
- Primary DI / UDI-DI
- 00850301007778
- FDA product code
- ITG
- GMDN term
- Pressure bandage, non-latex, reusable
- Device class
- Class I
- Regulation number
- 890.3025
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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