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Molecular Testing Labs

FDA UDI

by Blackfly Investments, LLC

Identity

Trade Name
Molecular Testing Labs FDA UDI
Generic Name
General-purpose absorbent tip applicator/swab, single-use FDA UDI
Device Name
Dried Blood Spot, Urine, and Swab Collection Kit FDA UDI
Model / Reference
Dried Blood Spot, Urine, and Swab Collection Kit FDA UDI
Description
Dried Blood Spot, Urine, and Swab Collection Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00860008357892 FDA UDI
GMDN Term
General-purpose absorbent tip applicator/swab, single-use FDA UDI

Classification

Commercial Distribution
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

Yes

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

Category: General-purpose absorbent tip applicator/swab, single-useUrine specimen collection kit IVDDried blood spot collection card IVD

Molecular Testing Labs by Blackfly Investments, LLC — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dried blood spot collection card IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca8ada41-8d4c-4450-ac2f-3520f6798224 33 fields · synced Jun 8, 2026