90403 Shoulder Arthroscopy Kit

FDA UDI

Class I (US FDA UDI)

by Xodus Medical, Inc.

Identity

Trade Name: 90403 Shoulder Arthroscopy Kit FDA UDI
Generic Name: Upper-limb traction wrap/trap, single-use FDA UDI
Device Name: 90403 Shoulder Arthroscopy Kit FDA UDI
Model / Reference: 90403 FDA UDI
Description: 90403 Shoulder Arthroscopy Kit FDA UDI

Identifiers

Catalog Number: 90403 FDA UDI
Primary DI / UDI-DI: 00787551011654 FDA UDI
FDA Product Code: KQZ FDA UDI
GMDN Term: Upper-limb traction wrap/trap, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.5890 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: Upper-limb traction wrap/trap, single-use

90403 Shoulder Arthroscopy Kit by Xodus Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Upper-limb traction wrap/trap, single-use.

Top Shelf Orthopedics — Top Shelf Manufacturing, LLC · Class I
McConnell Orthopedic MFG. CO. — MCCONNELL ORTHOPEDIC MFG. CO. · Class I
Medline — MEDLINE INDUSTRIES, INC. · Class I
McConnell Orthopedic MFG. CO. — MCCONNELL ORTHOPEDIC MFG. CO. · Class I
SchureMed — SCHUERCH CORPORATION · Class I
SchureMed — SCHUERCH CORPORATION · Class I
SchureMed — SCHUERCH CORPORATION · Class I
SchureMed — SCHUERCH CORPORATION · 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: Xodus Medical, Inc.

Sources (1)

FDA UDI 594a87dd-64e7-425e-b7ee-56dd7df9cbb7 35 fields · synced Jun 8, 2026