← Back to catalogue

Adhesion Microscope Slides

EUDAMEDFDA UDI

Class A (EU MDR)

Ref B9992010GL

by New Erie Scientific LLC

Identity

Trade Name
Adhesion Microscope Slides EUDAMED
Epredia FDA UDI
Generic Name
General specimen microscopy slide IVD, single-use FDA UDI
Device Name
Microscope Slides EUDAMED
Model / Reference
B9992010GL EUDAMED
Adhesion Microscope Slides FDA UDI

Identifiers

Catalog Number
B9992010GL FDA UDI
Primary DI / UDI-DI
00810041331663 EUDAMEDFDA UDI
Basic UDI-DI
081004133NES001MN EUDAMED
Unit of Use DI
10810041331660 EUDAMED
FDA Product Code
KEW FDA UDI
EMDN Code
W0503900201 MICROSCOPE SLIDES EUDAMED
GMDN Term
General specimen microscopy slide IVD, single-use FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.3010 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General specimen microscopy slide IVD, single-use

Adhesion Microscope Slides by New Erie Scientific LLC — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen microscopy slide IVD, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000008165
Authorised Representative
Epredia Netherlands B.V. NL-AR-000001488

Sources (2)

  • EUDAMED 187f7afc-2730-416f-a6d6-8795683849db 61 fields · synced Jun 18, 2026
  • FDA UDI c966e3b9-e013-4379-b201-eae1df1943f3 33 fields · synced May 30, 2026