Millennium

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name: Millennium FDA UDI
Generic Name: Body aspiration needle, reusable FDA UDI
Device Name: Micro Injection Needle Style g LL FDA UDI
Model / Reference: 39-MIN21607LL FDA UDI
Description: Micro Injection Needle Style g LL FDA UDI

Identifiers

Primary DI / UDI-DI: 00190776195342 FDA UDI
FDA Product Code: GDM FDA UDI
GMDN Term: Body aspiration needle, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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Implantable

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Contains Latex

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Prescription Use

Yes

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Over-the-Counter

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Convenience Kit

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Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

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Lot / Batch Number

Yes

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Serial Number

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Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Body aspiration needle, reusable

A high-quality, reusable body aspiration needle designed for medical professionals to safely and effectively remove fluid from the body cavities or obtain biopsy specimens.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: AVALIGN TECHNOLOGIES, Inc.

Sources (1)

FDA UDI fb719d5f-7b91-4b28-be50-182479b72c3a 34 fields · synced Jul 30, 2026