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SCANLAN® Dilators

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 3003-395

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Dilators FDA UDI
SCANLAN® Needle Holders FDA UDI
Generic Name
Vascular dilator, reusable FDA UDI
Suturing needle holder, reusable FDA UDI
Device Name
SCANLAN® Special Garrett Vascular Dilator EUDAMED
SCANLAN® Puskas™ Jacobson Micro Needle Holder EUDAMED
Special Garrett Vascular Dilator FDA UDI
Puskas™ Jacobson Micro Needle Holder FDA UDI
Model / Reference
3003-395 EUDAMEDFDA UDI
9009-49G FDA UDI
Description
Special Garrett Vascular Dilator FDA UDI
Puskas™ Jacobson Micro Needle Holder FDA UDI

Identifiers

Catalog Number
9009-49G FDA UDI
3003-395 FDA UDI
Primary DI / UDI-DI
00846159031454 EUDAMEDFDA UDI
00846159022780 EUDAMEDFDA UDI
Basic UDI-DI
B-00846159031454 EUDAMED
B-00846159022780 EUDAMED
FDA Product Code
DWP FDA UDI
FHQ FDA UDI
EMDN Code
L031102 EXPLORATION PROBES, REUSABLE EUDAMED
L0205 NEEDLE HOLDERS, REUSABLE EUDAMED
GMDN Term
Vascular dilator, reusable FDA UDI
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Class II FDA UDI
Regulation Number
870.4475 FDA UDI
876.4730 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: Vascular dilator, reusable

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

Similar devices

Also classified as Vascular dilator, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (4)

  • FDA UDI c827571a-ac00-447d-a14f-bb6630bdbcf9 35 fields · synced Jun 18, 2026
  • FDA UDI 79cfa304-bfea-46e1-a7d2-ef02ce6199a0 35 fields · synced May 30, 2026
  • EUDAMED 43316d42-97e4-4529-8c24-ea01766bec0f 61 fields · synced Jun 11, 2026
  • EUDAMED 3f49c2a1-c064-4b49-8043-6b1f471a4254 61 fields · synced Jun 18, 2026