Medline ES0101R
Medline ES0101R is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 12 May 2022 (UDI-DI 10888277326125), 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 | Number10888277326125 | Date12 May 2022 | StatusListed |
Official records
- AccessGUDID record 10888277326125
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Medline
- Generic name
- Rigid endoscopic scissors, single-use
- Model / Ref / Catalog
- ES0101R
- Primary DI / UDI-DI
- 10888277326125
- FDA product code
- NUJ
- GMDN term
- Rigid endoscopic scissors, single-use
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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