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Kit, Printer, Lp35

FDA UDI

Class I (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
KIT, PRINTER, LP35 FDA UDI
Generic Name
Thermal printer FDA UDI
Device Name
KIT, PRINTER, LP35 FDA UDI
Model / Reference
11335 FDA UDI
Description
KIT, PRINTER, LP35 FDA UDI

Identifiers

Catalog Number
11335-000005 FDA UDI
Primary DI / UDI-DI
00883873777237 FDA UDI
FDA Product Code
DSF FDA UDI
GMDN Term
Thermal printer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.2810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Thermal printer

Kit, Printer, Lp35 by PHYSIO-CONTROL, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thermal printer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 19ba4de8-2c2e-4c56-a271-ead8b1c6c2c8 35 fields · synced Jul 8, 2026