Novo Surgical Inc.

FDA UDI

Class I (US FDA UDI)

by Novo Surgical, Inc.

Identity

Trade Name: Novo Surgical Inc. FDA UDI
Generic Name: Coronary artery exposure retractor FDA UDI
Device Name: parsonnet epicardial retractor, 3x3 sharp prongs, 1" (25.0 mm), gold plated FDA UDI
Model / Reference: C6668-50G FDA UDI
Description: parsonnet epicardial retractor, 3x3 sharp prongs, 1" (25.0 mm), gold plated FDA UDI

Identifiers

Primary DI / UDI-DI: 00842331190186 FDA UDI
FDA Product Code: DWS FDA UDI
GMDN Term: Coronary artery exposure retractor FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 870.4500 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

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Coronary artery exposure retractor

Novo Surgical Inc. by Novo Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Novo Surgical, Inc.

Sources (1)

FDA UDI d6845aaa-955c-4b3c-9010-2fac4471787d 34 fields · synced May 30, 2026