Medline SCD48RH
Medline SCD48RH is a device classified as Unclassified made by Medline Industries, Inc., cleared under FDA 510(k) K170955 on 3 Jul 2017 and listed in FDA GUDID since 29 Jan 2025 (UDI-DI 10888277681552), 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 | Number10888277681552 | Date29 Jan 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK170955 | Date3 Jul 2017 | StatusActive |
Official records
- AccessGUDID record 10888277681552
- FDA 510(k) database K170955
Across registries
- FDA 510(k) K170955 decided 3 Jul 2017 Active
- FDA GUDID UDI-DI 10888277681552 listed 29 Jan 2025 Listed
Timeline
- Cleared FDA 510(k) K170955
- Listed FDA GUDID 10888277681552
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Medline
- Generic name
- Laparoscopic blunt dissector
- Model / Ref / Catalog
- SCD48RH
- Description
- SCD48 @SONICISION CORDLESS ULTRASONIC D
- Primary DI / UDI-DI
- 10888277681552
- 510(k) Number
- FDA product code
- NLQ
- GMDN term
- Laparoscopic blunt dissector
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
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