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TIC® 10 µL Capillary Pack (Plastic)

FDA UDI

Class I (US FDA UDI)

by BIOANALYTIC GmbH, biomed. Analysentechnik

Identity

Trade Name
TIC® 10 µL Capillary Pack (Plastic) FDA UDI
Generic Name
Microcapillary blood collection tube IVD, no additive FDA UDI
Model / Reference
TIC-CP10P FDA UDI

Identifiers

Primary DI / UDI-DI
04061609000514 FDA UDI
FDA Product Code
GIO FDA UDI
GMDN Term
Microcapillary blood collection tube IVD, no additive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6150 FDA UDI
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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Microcapillary blood collection tube IVD, no additive

TIC® 10 µL Capillary Pack (Plastic) by BIOANALYTIC GmbH, biomed. Analysentechnik — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microcapillary blood collection tube IVD, no additive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
BIOANALYTIC GmbH, biomed. Analysentechnik

Sources (1)

  • FDA UDI 14d2676f-eb60-4000-b930-6d1e81fb8b5f 32 fields · synced May 30, 2026