Novocart

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name: NOVOCART FDA UDI
Generic Name: Bone curette, reusable FDA UDI
Device Name: NOVOCART Cartilage Curette, angled, 8 3/4", (220 mm), rectangular, bilateral sharp tip, peek handle, width: 4 mm, non-sterile, reusable FDA UDI
Model / Reference: FR740R FDA UDI
Description: NOVOCART Cartilage Curette, angled, 8 3/4", (220 mm), rectangular, bilateral sharp tip, peek handle, width: 4 mm, non-sterile, reusable FDA UDI

Identifiers

Catalog Number: FR740R FDA UDI
Primary DI / UDI-DI: 04046963315528 FDA UDI
FDA Product Code: FZS FDA UDI
GMDN Term: Bone curette, 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

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone curette, reusable

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

Similar devices

Also classified as Bone curette, reusable.

Symmetry Bruns — SYMMETRY SURGICAL INC. · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Spinal System — BIOMET SPINE LLC · Class I
Life Instruments — Life Instrument Corporation · Class I
Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
Novo Surgical — NOVO SURGICAL, INC. · Class I
Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
Volkmann Bone Curette Oval - Fig. 00 17 cm - 6 3/4" Scoop Size 4.4 mm Stainless Steel — SURTEX INSTRUMENTS LTD · 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: Aesculap, Inc.

Sources (1)

FDA UDI a0f7d349-3d87-4e15-ac04-4e136c26f443 35 fields · synced May 30, 2026