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SCANLAN® M.D. Retractor Arm

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 8008-932L

by Scanlan International Inc

Identity

Trade Name
SCANLAN® M.D. Retractor Arm FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
SCANLAN® M.D. Titanium Retractor Arm EUDAMED
SCANLAN® M.D. Retractor Arm Size 2 Left FDA UDI
Model / Reference
8008-932L EUDAMEDFDA UDI
Description
SCANLAN® M.D. Retractor Arm Size 2 Left FDA UDI

Identifiers

Catalog Number
8008-932L FDA UDI
Primary DI / UDI-DI
00846159034530 EUDAMEDFDA UDI
Basic UDI-DI
B-00846159034530 EUDAMED
FDA Product Code
GAD FDA UDI
EMDN Code
L03140199 SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical retractor/retraction system blade, 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 retractor/retraction system blade, reusable

SCANLAN® M.D. Retractor Arm by Scanlan International Inc — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, 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 40e80262-be16-40e7-931e-1793d642cbd7 35 fields · synced Jul 20, 2026
  • EUDAMED b83d079f-8a4d-480d-9c3d-ad28f7b94009 61 fields · synced Jul 20, 2026