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Histobond Float ~76x51x1 fbk 2xMR V=50 Superior CE

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 082999093

by Paul Marienfeld GmbH & Co. KG

Identity

Trade Name
Histobond Float ~76x51x1 fbk 2xMR V=50 Superior CE EUDAMED
Marienfeld Superior FDA UDI
Generic Name
General specimen microscopy slide IVD, single-use FDA UDI
Device Name
Special size microscopy Slides (IVD) EUDAMED
Model / Reference
082999093 EUDAMED
HistoBond ~76x51x1 ground edges 2xmarking area FDA UDI

Identifiers

Catalog Number
082999093 FDA UDI
Primary DI / UDI-DI
04064279017295 EUDAMEDFDA UDI
Basic UDI-DI
4250317302OTONUT EUDAMED
Unit of Use DI
04064279017400 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
Germany 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

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

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

Histobond Float ~76x51x1 fbk 2xMR V=50 Superior CE by Paul Marienfeld GmbH & Co. KG — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID

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
DE-MF-000023724

Sources (2)

  • EUDAMED f9bcab32-1a06-4903-bdaa-25f0e5ba5e42 61 fields · synced Jun 19, 2026
  • FDA UDI 17d30529-e4fc-41ad-b456-4d016567e71c 33 fields · synced May 30, 2026