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Aerospray 30 Slide Carousel

EUDAMEDFDA UDI

Class A (EU MDR)

Ref AC-189Model Aerospray

by ELITechGroup Inc.

Identity

Trade Name
Aerospray 30 Slide Carousel EUDAMED
30-slide vented carousel for Aerospray® FDA UDI
Generic Name
Microscope slide stainer IVD FDA UDI
Device Name
A 30-slide vented carousel to be used with Aerospray® stainer/cytocentrifuges to facilitate the staining of biological samples. FDA UDI
Model / Reference
Aerospray EUDAMED
AC-189 EUDAMEDFDA UDI
Description
A 30-slide vented carousel to be used with Aerospray® stainer/cytocentrifuges to facilitate the staining of biological samples. FDA UDI

Identifiers

Primary DI / UDI-DI
03661540300028 EUDAMEDFDA UDI
Basic UDI-DI
3661540AerosprayG8 EUDAMED
FDA Product Code
KPA FDA UDI
EMDN Code
W0202059002 AUTOMATED SLIDE STAINERS EUDAMED
GMDN Term
Microscope slide stainer IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.3800 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Microscope slide stainer IVD

Aerospray 30 Slide Carousel by Elitechgroup Inc. — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microscope slide stainer IVD.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ELITechGroup Inc.
EUDAMED SRN
US-MF-000006942
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (2)

  • EUDAMED 56f3297f-7c29-4fe7-b114-730d85c8ad4e 61 fields · synced Jun 20, 2026
  • FDA UDI fc847fb6-116c-4b1e-9976-bbf942f1b8d4 34 fields · synced May 30, 2026