Long Cervical Micro-Bayonet Curette Set

FDA UDI

Class I (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name: Long Cervical Micro-Bayonet Curette Set FDA UDI
Generic Name: General-purpose curette FDA UDI
Device Name: Aescalap Type Long Cervical Micro-Bayonet Curette Set Consists of the Following: 1 x 7418-10L, 1 x 7418-20L, 1 x 7418-30L, 1 x 7418-40L, 1 x 7418-80L, 1 x 7418-12L, 1 x 7418-22L, 1 x 7418-32L, 1 x 7418-42L, 1 x 7418-82L, 1 x 7418-14L, 1 x 7418-24L, 1 x 7418-34L, 1 x 7418-44L, 1 x 7418-84L, 1 x 7418-16L, 1 x 7418-26L, 1 x 7418-36L, 1 x 7418-46L, 1 x 7418-91L, 1 x 7418-92L, 1 x 7418-93 & 1 x 7418-95 FDA UDI
Model / Reference: 7418-00L FDA UDI
Description: Aescalap Type Long Cervical Micro-Bayonet Curette Set Consists of the Following: 1 x 7418-10L, 1 x 7418-20L, 1 x 7418-30L, 1 x 7418-40L, 1 x 7418-80L, 1 x 7418-12L, 1 x 7418-22L, 1 x 7418-32L, 1 x 7418-42L, 1 x 7418-82L, 1 x 7418-14L, 1 x 7418-24L, 1 x 7418-34L, 1 x 7418-44L, 1 x 7418-84L, 1 x 7418-16L, 1 x 7418-26L, 1 x 7418-36L, 1 x 7418-46L, 1 x 7418-91L, 1 x 7418-92L, 1 x 7418-93 & 1 x 7418-95 FDA UDI

Identifiers

Catalog Number: 7418-00L FDA UDI
Primary DI / UDI-DI: 10840199543752 FDA UDI
FDA Product Code: FZS FDA UDI
GMDN Term: General-purpose curette 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: Bone curette, reusable General-purpose curette Ophthalmic curette, reusable

Long Cervical Micro-Bayonet Curette Set by Koros USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Ophthalmic curette, reusable.

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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: Koros USA, Inc.

Sources (1)

FDA UDI 703a0840-3187-4f7d-99de-a3a0cb50e198 37 fields · synced Jun 8, 2026