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SCANLAN® Forceps

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 4004-250

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Forceps FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
SCANLAN® Micro Forceps EUDAMED
Lightweight, Round Handle, Straight, 1 mm Diamond Dust™ ring tips, 7 1/8" / 18.1 cm FDA UDI
Model / Reference
4004-250 EUDAMEDFDA UDI
Description
Lightweight, Round Handle, Straight, 1 mm Diamond Dust™ ring tips, 7 1/8" / 18.1 cm FDA UDI

Identifiers

Catalog Number
4004-250 FDA UDI
Primary DI / UDI-DI
00846159009699 EUDAMEDFDA UDI
Basic UDI-DI
B-00846159009699 EUDAMED
FDA Product Code
GEN 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
878.4800 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® Forceps by Scanlan International Inc — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

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 5d4ebc83-c472-483d-9e78-22ac98010f6b 35 fields · synced Jun 19, 2026
  • EUDAMED 16e0c7db-9e6f-45c1-b329-a318b1ba266b 61 fields · synced Jun 19, 2026