Aqualoc®

FDA UDI

Class I (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name: AQUALOC® FDA UDI
Generic Name: Arthroscopic obturator FDA UDI
Model / Reference: 900382 FDA UDI

Identifiers

Catalog Number: 900382 FDA UDI
Primary DI / UDI-DI: 00880304476233 FDA UDI
FDA Product Code: NBH FDA UDI
GMDN Term: Arthroscopic obturator FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1100 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: Arthroscopic obturator

Aqualoc® by Biomet Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class I
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ZEOS — SANTA BARBARA IMAGING SYSTEMS, INC. · 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

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Manufacturer

Manufacturer: Biomet Orthopedics, Inc.

Sources (1)

FDA UDI dd3c439d-da53-4b2c-bda9-88a090ca2423 35 fields · synced May 30, 2026