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Macro & Micro-Test Sample Release Reagent

FDA UDIEUDAMED

Class I (US FDA UDI)

by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.

Identity

Trade Name
Macro & Micro-Test Sample Release Reagent FDA UDI
Generic Name
Nucleic acid extraction/isolation kit IVD FDA UDI
Model / Reference
50 tests/kit FDA UDI

Identifiers

Primary DI / UDI-DI
06974849369045 FDA UDI
FDA Product Code
JJH FDA UDI
GMDN Term
Nucleic acid extraction/isolation kit IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2310 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nucleic acid extraction/isolation kit IVD

Macro & Micro-Test Sample Release Reagent by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd. — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Nucleic acid extraction/isolation kit 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 9d670f56-f3e7-40c6-adc9-58241b1c3474 32 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026