← Back to catalogue

Forcep

FDA UDI

Class I (US FDA UDI)

by Koros USA, Inc.

Identity

Trade Name
Forcep FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
Micro Forceps Straight Platfrom Titanium 0.4mm Tip, 17.5cm 7" FDA UDI
Model / Reference
8046-18T FDA UDI
Description
Micro Forceps Straight Platfrom Titanium 0.4mm Tip, 17.5cm 7" FDA UDI

Identifiers

Catalog Number
8046-18T FDA UDI
Primary DI / UDI-DI
10840199534057 FDA UDI
FDA Product Code
HTC FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Forcep by Koros USA, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, tweezers-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Koros USA, Inc.

Sources (1)

  • FDA UDI e75eaef9-fee0-44ae-8461-6be6a93946ea 36 fields · synced Jun 6, 2026