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75mm Hemato-clad Heparinized

FDA UDI

Class II (US FDA UDI)

by Drummond Scientific Company

Identity

Trade Name
75mm Hemato-clad Heparinized FDA UDI
Generic Name
Capillary blood collection tube IVD, ammonium heparin FDA UDI
Device Name
Capillary Tubes FDA UDI
Model / Reference
1-000-7500-HC FDA UDI
Description
Capillary Tubes FDA UDI

Identifiers

Catalog Number
1-000-7500-HC/5 FDA UDI
Primary DI / UDI-DI
00860001024012 FDA UDI
FDA Product Code
GHY FDA UDI
GMDN Term
Capillary blood collection tube IVD, ammonium heparin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6400 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

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

Category: Capillary blood collection tube IVD, ammonium heparin

75mm Hemato-clad Heparinized by Drummond Scientific Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Capillary blood collection tube IVD, ammonium heparin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 15de693b-1af0-4748-a253-fe2525230d2e 35 fields · synced May 29, 2026