Cable, Printer, LP35 11330
Ref 11330-000014Model 08858251028268UW
Cable, Printer, LP35 (11330-000014) is a thermal printer (EU MDR Class I; FDA Class I; FDA product code DSF, Recorder, Paper Chart) made by PHYSIO-CONTROL, Inc., registered in EUDAMED on 26 Sep 2026 (Basic UDI-DI 08858251028268UW) and listed in FDA GUDID since 19 Jun 2024 (UDI-DI 00883873834374), active as of 24 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 | Number08858251028268UW 00883873834374 | Date26 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00883873834374 | Date19 Jun 2024 | StatusListed |
Official records
- EUDAMED public site 08858251028268UW
- AccessGUDID record 00883873834374
Across registries
- EUDAMED Basic UDI-DI 08858251028268UW registered 26 Sep 2026 Active
- FDA GUDID UDI-DI 00883873834374 listed 19 Jun 2024 Listed
Timeline
- Listed FDA GUDID 00883873834374
- Registered EUDAMED 08858251028268UW
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Cable, Printer, LP35
- Generic name
- Thermal printer
- Device name
- LIFEPAK 35 Printer Cable
- Model / Ref / Catalog
- 08858251028268UW, 11330-000014, 11330
- Primary DI / UDI-DI
- 00883873834374
- Basic UDI-DI
- 08858251028268UW
- Direct marketing DI
- 00883873834374
- FDA product code
- DSF
- EMDN code
- Z12030580 Defibrillators - hardware accessories
- GMDN term
- Thermal printer
- Device class
- Class I
- Regulation number
- 870.2810
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 08858251028268UW 11330-000014 | 11330 |
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