Medline MDG7101000
Medline MDG7101000 is a Class II device made by Medline Industries, Inc., cleared under FDA 510(k) K060233 on 19 Jul 2006 and listed in FDA GUDID since 29 Mar 2022 (UDI-DI 10888277122246), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10888277122246 | Date29 Mar 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK060233 | Date19 Jul 2006 | StatusActive |
Official records
- AccessGUDID record 10888277122246
- FDA 510(k) database K060233
Across registries
- FDA 510(k) K060233 decided 19 Jul 2006 Active
- FDA GUDID UDI-DI 10888277122246 listed 29 Mar 2022 Listed
Timeline
- Cleared FDA 510(k) K060233
- Listed FDA GUDID 10888277122246
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Medline
- Generic name
- Rigid endoscope telescope
- Model / Ref / Catalog
- MDG7101000
- Primary DI / UDI-DI
- 10888277122246
- 510(k) Number
- FDA product code
- GCJ
- GMDN term
- Rigid endoscope telescope
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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