Millennium

FDA UDI

Class II (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name: Millennium FDA UDI
Generic Name: Surgical bulldog clamp, reusable FDA UDI
Device Name: Angled Single Clamp pair vein/artery size 1.0mm-2.25mm FDA UDI
Model / Reference: 18-DC3 FDA UDI
Description: Angled Single Clamp pair vein/artery size 1.0mm-2.25mm FDA UDI

Identifiers

Primary DI / UDI-DI: 00190776155247 FDA UDI
FDA Product Code: DXC FDA UDI
GMDN Term: Surgical bulldog clamp, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.4450 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

FDA UDI

Prescription Use

Yes

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Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

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Premarket Exempt

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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: Surgical bulldog clamp, reusable

Millennium by AVALIGN TECHNOLOGIES, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Clamp, Hysterectomy, model Z 30.5cm strongly curved shanks angled — Geister Medizin Technik GmbH · Class I

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 II	Pending data

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Manufacturer

Manufacturer: AVALIGN TECHNOLOGIES, Inc.

Sources (1)

FDA UDI f4e87cec-fb26-40fe-95c3-7020619a1577 34 fields · synced May 30, 2026