Millennium

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name: Millennium FDA UDI
Generic Name: Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name: 3.4MM HEUWIESER NASAL BITE FCPS OVAL STR 10" SHAFT 13"OL FDA UDI
Model / Reference: 72-42452801 FDA UDI
Description: 3.4MM HEUWIESER NASAL BITE FCPS OVAL STR 10" SHAFT 13"OL FDA UDI

Identifiers

Primary DI / UDI-DI: 00190776389970 FDA UDI
FDA Product Code: LRC FDA UDI
GMDN Term: Rigid endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscopic biopsy forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic biopsy forceps, reusable.

RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
MaxMoreSpine — Hoogland Spine Products, GmbH · Class I
JACKSON BIOPSY FORCEPS — SONTEC INSTRUMENTS, INC. · Class I
Hermann Medizintechnik GmbH — Hermann Medizintechnik GmbH · Class II
MaxMoreSpine — Hoogland Spine Products, GmbH · Class I
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
ELMED — ELMED INCORPORATED · Class II
MaxMoreSpine — Hoogland Spine Products, 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 I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: AVALIGN TECHNOLOGIES, Inc.

Sources (1)

FDA UDI 0e4c7abc-f325-49cd-83bd-1f1f11619fad 34 fields · synced May 30, 2026