Spand-Gel SPHD28
by Medi-Tech International Corporation
Spand-Gel SPHD28 is a Class I device made by Medi-Tech International Corporation, listed in FDA GUDID since 11 Jun 2019 (UDI-DI 00027479260049), registry data as of 23 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 | Number00027479260049 | Date11 Jun 2019 | StatusListed |
Official records
- AccessGUDID record 00027479260049
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Spand-Gel
- Generic name
- Wound hydrogel dressing, non-sterile
- Model / Ref / Catalog
- SPHD28
- Primary DI / UDI-DI
- 00027479260049
- FDA product code
- NAE
- GMDN term
- Wound hydrogel dressing, non-sterile
- Device class
- Class I
- Regulation number
- 878.4022
- GUDID distribution status
- In Commercial Distribution
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