AVR S-S Tower Attachment Set

FDA UDI

Class I (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name: AVR S-S Tower Attachment Set FDA UDI
Generic Name: Self-retaining surgical retractor, reusable FDA UDI
Device Name: AVR S-S Tower Attachment Set, Consists of the Following: 1 x 8950-15 AVR Super-Slide Tower , 2 x 8950-20 AVR Super-Slide Arm w/ 2 Connecting Clamps, 1 x 8950-22 AVR Super-Slide Mitral Valve Retractor Small 20mm Wide, 1 x 8950-24 AVR Super-Slide Mitral Valve Retractor Medium 22.5mm Wide & 1 x 8950-26 AVR Super-Slide Mitral Valve Retractor Large 28mm Wide FDA UDI
Model / Reference: 8950-75 FDA UDI
Description: AVR S-S Tower Attachment Set, Consists of the Following: 1 x 8950-15 AVR Super-Slide Tower , 2 x 8950-20 AVR Super-Slide Arm w/ 2 Connecting Clamps, 1 x 8950-22 AVR Super-Slide Mitral Valve Retractor Small 20mm Wide, 1 x 8950-24 AVR Super-Slide Mitral Valve Retractor Medium 22.5mm Wide & 1 x 8950-26 AVR Super-Slide Mitral Valve Retractor Large 28mm Wide FDA UDI

Identifiers

Catalog Number: 8950-75 FDA UDI
Primary DI / UDI-DI: 10840199538444 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Self-retaining surgical retractor, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Self-retaining surgical retractor, reusable

AVR S-S Tower Attachment Set by Koros USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-retaining surgical retractor, reusable.

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Avalign — AVALIGN TECHNOLOGIES, Inc. · Class II
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Symmetry Cloward — SYMMETRY SURGICAL INC. · Class II
Life Instruments — Life Instrument Corporation · Class I
Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
SELF RETAINING CORONOID RETRACTOR CHAIN WITH RINGS — W.H. Holden, 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: Koros USA, Inc.

Sources (1)

FDA UDI 9133d215-12d3-4d3c-b0f7-151ef7fa746d 37 fields · synced May 30, 2026