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ThunderBolt EIA (CLIA)

FDA UDIEUDAMED

Class I (US FDA UDI)

by Gold Standard Diagnostics, LLC

Identity

Trade Name
ThunderBolt EIA (CLIA) FDA UDI
Generic Name
Enzyme immunoassay (EIA) analyser IVD FDA UDI
Device Name
ThunderBolt EIA-CLIA (refurbished) FDA UDI
Model / Reference
00300-CLR FDA UDI
Description
ThunderBolt EIA-CLIA (refurbished) FDA UDI

Identifiers

Catalog Number
00300-CLR FDA UDI
Primary DI / UDI-DI
B35000300CLR0 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Enzyme immunoassay (EIA) analyser IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 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

No

FDA UDI

Category: Chemiluminescent immunoassay analyser IVDEnzyme immunoassay (EIA) analyser IVD

ThunderBolt EIA (CLIA) by Gold Standard Diagnostics, LLC — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Enzyme immunoassay (EIA) analyser IVD.

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 5690960a-4d56-4986-8830-314a99998c7f 34 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026