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SCANLAN® Retractors

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 8008-73

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Retractors FDA UDI
Generic Name
Self-retaining surgical retractor, reusable FDA UDI
Device Name
SCANLAN® Finochietto Retractor EUDAMED
Finochietto Retractor, Aluminum, Baby Size, Concave-Convex Blades, 60 mm Long x 15 mm Deep, Arms 150 mm Long, Spread 120 mm FDA UDI
Model / Reference
8008-73 EUDAMEDFDA UDI
Description
Finochietto Retractor, Aluminum, Baby Size, Concave-Convex Blades, 60 mm Long x 15 mm Deep, Arms 150 mm Long, Spread 120 mm FDA UDI

Identifiers

Catalog Number
8008-73 FDA UDI
Primary DI / UDI-DI
00846159035353 EUDAMEDFDA UDI
Basic UDI-DI
B-00846159035353 EUDAMED
FDA Product Code
GAD FDA UDI
EMDN Code
L03140199 SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHER EUDAMED
GMDN Term
Self-retaining surgical retractor, 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: Self-retaining surgical retractor, reusable

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

Similar devices

Also classified as Self-retaining surgical retractor, 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 46f2b1c6-f030-4753-ac83-a41e04ac0423 35 fields · synced Jul 16, 2026
  • EUDAMED 91ae1a8a-7e98-4e8d-9bd4-d9bb1208dd5a 61 fields · synced Jul 16, 2026