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Hmg

FDA UDI

Class II (US FDA UDI)

by Hartman Medical Group, LLC

Identity

Trade Name
HMG FDA UDI
Generic Name
Intravenous administration tubing extension set FDA UDI
Device Name
Macro Bore IV extension set with Needleless Y-site and removable Needleless Connector FDA UDI
Model / Reference
001 FDA UDI
Description
Macro Bore IV extension set with Needleless Y-site and removable Needleless Connector FDA UDI

Identifiers

Primary DI / UDI-DI
10850048235059 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Intravenous administration tubing extension set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intravenous administration tubing extension set

Hmg by Hartman Medical Group, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous administration tubing extension set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hartman Medical Group, LLC

Sources (1)

  • FDA UDI d7bc9026-264e-4bf9-836c-089527edc683 33 fields · synced May 30, 2026