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SCANLAN® Scanturian™ MIS Instrument

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 9019-420-25

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Scanturian™ MIS Instrument FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
SCANLAN® Scanturian™ MIS DeBakey Forceps EUDAMED
SCANLAN® Scanturian™ MIS Forceps FDA UDI
Model / Reference
9019-420-25 EUDAMEDFDA UDI
Description
SCANLAN® Scanturian™ MIS Forceps FDA UDI

Identifiers

Catalog Number
9019-420-25 FDA UDI
Primary DI / UDI-DI
00846159034165 EUDAMEDFDA UDI
Basic UDI-DI
B-00846159034165 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® Scanturian™ MIS Instrument 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 bf6d7b4b-27ea-4e49-8e22-fd9b84e0740c 36 fields · synced Jul 14, 2026
  • EUDAMED 12b831e0-e7db-4aae-bcec-a5ef362320c9 61 fields · synced Jul 14, 2026