Millennium

FDA UDI

Class II (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name: Millennium FDA UDI
Generic Name: Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name: 10mm 45cm Biopsy Spoon Forceps, Short, Single Action, 10mm Tip Rotatable 1-Piece w/Flush Port, Type 16 handle - Modified to have Stainless Steel Shaft. Spring Handle FDA UDI
Model / Reference: 72-5210137B16M FDA UDI
Description: 10mm 45cm Biopsy Spoon Forceps, Short, Single Action, 10mm Tip Rotatable 1-Piece w/Flush Port, Type 16 handle - Modified to have Stainless Steel Shaft. Spring Handle FDA UDI

Identifiers

Primary DI / UDI-DI: 00190776410582 FDA UDI
FDA Product Code: GEI FDA UDI
GMDN Term: Rigid endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4400 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

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

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 II — 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 II	Pending data

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

Manufacturer

Manufacturer: AVALIGN TECHNOLOGIES, Inc.

Sources (1)

FDA UDI 8bd5b82a-edf3-4256-9611-e070bed14385 34 fields · synced May 30, 2026