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SCANLAN® Thoracoscopic Dissector

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 9009-214

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Thoracoscopic Dissector FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
SCANLAN® Gonzalez-Rivas EUDAMED
Thoracoscopic GR Debakey CLP Dissector, 5-7mm, Tapered Shaft, W/ ratchet, 24CM WL, 34CM TL FDA UDI
Model / Reference
9009-214 EUDAMEDFDA UDI
Description
Thoracoscopic GR Debakey CLP Dissector, 5-7mm, Tapered Shaft, W/ ratchet, 24CM WL, 34CM TL FDA UDI

Identifiers

Catalog Number
9009-214 FDA UDI
Primary DI / UDI-DI
00846159033120 EUDAMEDFDA UDI
Basic UDI-DI
B-00846159033120 EUDAMED
510(k) Number
K945474 FDA UDI
FDA Product Code
GCJ FDA UDI
EMDN Code
L031306 HEMOSTATIC FORCEPS, REUSABLE EUDAMED
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

SCANLAN® Thoracoscopic Dissector by Scanlan International Inc — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 4c7b95c0-f83a-457b-9be8-4c508613a8ed 36 fields · synced Jul 20, 2026
  • EUDAMED 24f9995c-d184-46d1-8d3e-3c06c7333f48 61 fields · synced Jul 20, 2026