← Back to catalogue

Leica ASP300 S

FDA UDIEUDAMED

Class I (US FDA UDI)

by Leica Biosystems Nussloch GmbH

Identity

Trade Name
Leica ASP300 S FDA UDI
Generic Name
Tissue processor IVD, automated/semi-automated FDA UDI
Device Name
The instrument has been designed so that it is safe to use by the operator as well as for process¬ing specimens – provided that it is operated according to the present Instructions for Use. The Leica ASP300 S is a modular tissue processor for the following laboratory applications: • Fixation • Dehydration • Paraffin infiltration of histological tissue specimens. FDA UDI
Model / Reference
000000014047643515 FDA UDI
Description
The instrument has been designed so that it is safe to use by the operator as well as for process¬ing specimens – provided that it is operated according to the present Instructions for Use. The Leica ASP300 S is a modular tissue processor for the following laboratory applications: • Fixation • Dehydration • Paraffin infiltration of histological tissue specimens. FDA UDI

Identifiers

Catalog Number
14047643515 FDA UDI
Primary DI / UDI-DI
04049188055965 FDA UDI
FDA Product Code
IEO FDA UDI
GMDN Term
Tissue processor IVD, automated/semi-automated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3875 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tissue processor IVD, automated/semi-automated

Leica ASP300 S by Leica Biosystems Nussloch GmbH — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Tissue processor IVD, automated/semi-automated.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 2ee81f15-e304-44b6-adc7-125979523923 37 fields · synced Jun 17, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026