Medline DYNDCLO1000
Ref DYNDCLO1000
Medline DYNDCLO1000 is a device classified as Class I in the EU and Class II in the US made by Medline Industries, Inc., registered in EUDAMED on 15 Jul 2026 (Basic UDI-DI 0080196DC265NSZS) and listed in FDA GUDID since 25 Oct 2024 (UDI-DI 40080196140184), active as of 25 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0080196DC265NSZS 40080196140184 | Date15 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number40080196140184 | Date25 Oct 2024 | StatusListed |
Official records
- EUDAMED public site 0080196DC265NSZS
- AccessGUDID record 40080196140184
Across registries
- EUDAMED Basic UDI-DI 0080196DC265NSZS registered 15 Jul 2026 Active
- FDA GUDID UDI-DI 40080196140184 listed 25 Oct 2024 Listed
Timeline
- Listed FDA GUDID 40080196140184
- Registered EUDAMED 0080196DC265NSZS
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Medline
- Generic name
- Suction/irrigation system canister/bottle holder, reusable
- Device name
- Suction canister
- Model / Ref / Catalog
- DYNDCLO1000
- Primary DI / UDI-DI
- 40080196140184
- Basic UDI-DI
- 0080196DC265NSZS
- Unit of use DI
- 10080196140183
- FDA product code
- KDQ
- EMDN code
- A06030401 Intraoperative suction containers
- GMDN term
- Suction/irrigation system canister/bottle holder, reusable
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 880.6740
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class I | Class II |
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