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RELY Mono

FDA UDI

Class II (US FDA UDI)

by Stanbio Laboratory, L.p.

Identity

Trade Name
RELY Mono FDA UDI
Generic Name
Epstein-Barr virus (EBV) heterophile antibody IVD, kit, rapid ICT, clinical FDA UDI
Device Name
For the Qualitative Detection of Infectious Mononucleosis (IM) Heterophile Antibodies in Whole blood, Serum or Plasma. FDA UDI
Model / Reference
6200-020 FDA UDI
Description
For the Qualitative Detection of Infectious Mononucleosis (IM) Heterophile Antibodies in Whole blood, Serum or Plasma. FDA UDI

Identifiers

Catalog Number
6200-020 FDA UDI
Primary DI / UDI-DI
00657498000038 FDA UDI
FDA Product Code
KTN FDA UDI
GMDN Term
Epstein-Barr virus (EBV) heterophile antibody IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5640 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

RELY Mono by Stanbio Laboratory, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ea85140c-ce20-403c-b01a-edc2fc1b805a 37 fields · synced May 30, 2026