PremierPro 26136
PremierPro 26136 is a Class I device made by Prestige Ameritech, listed in FDA GUDID since 30 Jul 2020 (UDI-DI 00818566011619), 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 | Number00818566011619 | Date30 Jul 2020 | StatusListed |
Official records
- AccessGUDID record 00818566011619
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PremierPro
- Generic name
- Isolation gown, single-use
- Model / Ref / Catalog
- 26136
- Primary DI / UDI-DI
- 00818566011619
- FDA product code
- LYU
- GMDN term
- Isolation gown, single-use
- Device class
- Class I
- Regulation number
- 878.4040
- GUDID distribution status
- In Commercial Distribution
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