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Immunofluorescence Reader

FDA UDIEUDAMED

Class II (US FDA UDI)

by Shenzhen YHLO Biotech Co., Ltd.

Identity

Trade Name
Immunofluorescence Reader FDA UDI
Generic Name
Fluorescent immunoassay analyser IVD, laboratory FDA UDI
Model / Reference
UNICELL-S FDA UDI

Identifiers

Catalog Number
F6101 FDA UDI
Primary DI / UDI-DI
06925912711087 FDA UDI
FDA Product Code
NSU FDA UDI
GMDN Term
Fluorescent immunoassay analyser IVD, laboratory FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.2570 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Fluorescent immunoassay analyser IVD, laboratory

Immunofluorescence Reader by Shenzhen YHLO Biotech Co., Ltd. — Class II — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Fluorescent immunoassay analyser IVD, laboratory.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 8df7418e-b45e-423c-b5c1-dc8c28b20120 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026