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Tasso+ Convenience Kit

FDA UDI

Class II (US FDA UDI)

by Tasso Inc.

Identity

Trade Name
Tasso+ Convenience Kit FDA UDI
Generic Name
Capillary blood collection system IVD FDA UDI
Model / Reference
K1019-04 FDA UDI

Identifiers

Primary DI / UDI-DI
00850038691042 FDA UDI
FDA Product Code
PQD FDA UDI
GMDN Term
Capillary blood collection system IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 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

Yes

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
Sterilization Method
Radiation Sterilization FDA UDI

Tasso+ Convenience Kit by Tasso Inc. — 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

Manufacturer
Tasso Inc.

Sources (1)

  • FDA UDI bd28f477-45a0-44c6-9950-2ba53d57c806 35 fields · synced May 30, 2026