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SCANLAN® Titanium Forceps

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 3003-916

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Titanium Forceps FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
SCANLAN® Titanium Micro Forceps EUDAMED
S LEGACY Mic fcp, RH, NS DG, str 1.0 mm DD pft, 9"/23 cm FDA UDI
Model / Reference
3003-916 EUDAMEDFDA UDI
Description
S LEGACY Mic fcp, RH, NS DG, str 1.0 mm DD pft, 9"/23 cm FDA UDI

Identifiers

Catalog Number
3003-916 FDA UDI
Primary DI / UDI-DI
00846159003871 EUDAMEDFDA UDI
Basic UDI-DI
B-00846159003871 EUDAMED
FDA Product Code
GZX FDA UDI
EMDN Code
L031306 HEMOSTATIC FORCEPS, REUSABLE EUDAMED
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
882.4525 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

Yes

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

SCANLAN Titanium Forceps is a high-grade, reusable surgical soft-tissue manipulation instrument designed for neurology procedures. Its tweezers-like design features variously designed tips at the working end, allowing for precise grasping and manipulation of delicate tissues. This instrument is not an electrosurgical device and is intended to be sterilized prior to use.

Similar devices

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

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 2f062829-3707-4bd0-976c-a6b20b4e4643 35 fields · synced Jul 29, 2026
  • EUDAMED 86c19968-b74a-457d-ac57-67dbea666481 61 fields · synced Jun 19, 2026