← Back to catalogue

SCANLAN® MicroSurgical Instruments

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 3003-183N

by Scanlan International Inc

Identity

Trade Name
SCANLAN® MicroSurgical Instruments FDA UDI
Generic Name
Open-surgery dissector FDA UDI
Device Name
SCANLAN® Aneurysm Ruler EUDAMED
SCANLAN ANEURYSM RULER CURVED BLUNT 1MM CALIBRATED TIP 7 1/4" / 18.5CM FDA UDI
Model / Reference
3003-183N EUDAMED
3784-121 FDA UDI
Description
SCANLAN ANEURYSM RULER CURVED BLUNT 1MM CALIBRATED TIP 7 1/4" / 18.5CM FDA UDI

Identifiers

Catalog Number
3784-121 FDA UDI
Primary DI / UDI-DI
00846159035261 EUDAMEDFDA UDI
Basic UDI-DI
B-00846159035261 EUDAMED
FDA Product Code
GZX FDA UDI
EMDN Code
L031102 EXPLORATION PROBES, REUSABLE EUDAMED
GMDN Term
Open-surgery dissector 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: Open-surgery dissector

SCANLAN® MicroSurgical Instruments by Scanlan International Inc — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery dissector.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI aafbc324-9530-4cad-838f-4f045d327ae7 35 fields · synced Jun 11, 2026
  • EUDAMED 220f099d-fa6c-44cc-968a-f1afc3df493e 61 fields · synced Jun 11, 2026