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White Poplar, Populus alba

FDA UDI

Class I (US FDA UDI)

by Hycor Biomedical Llc

Identity

Trade Name
White Poplar, Populus alba FDA UDI
Generic Name
Assay development analyte-specific reagent IVD FDA UDI
Model / Reference
T96 FDA UDI

Identifiers

Catalog Number
744100 FDA UDI
Primary DI / UDI-DI
00816879026504 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Assay development analyte-specific reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 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

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

No

FDA UDI

White Poplar, Populus alba by Hycor Biomedical Llc — Class I — 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 18bae451-a648-4cca-a9cc-b98823bb203d 36 fields · synced Jun 1, 2026