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SCANLAN® Surgical skin markers

FDA UDI

Class I (US FDA UDI)

by Scanlan International Inc

Identity

Trade Name
SCANLAN® Surgical skin markers FDA UDI
Generic Name
Skin marking pen, single-use FDA UDI
Device Name
SCANLAN® Surgical skin markers - Regular Tip, Gentian Violet (1 per sterile package with ruler) FDA UDI
Model / Reference
1001-710 FDA UDI
Description
SCANLAN® Surgical skin markers - Regular Tip, Gentian Violet (1 per sterile package with ruler) FDA UDI

Identifiers

Catalog Number
1001-710 FDA UDI
Primary DI / UDI-DI
00846159000368 FDA UDI
FDA Product Code
FZZ FDA UDI
GMDN Term
Skin marking pen, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin marking pen, single-use

SCANLAN® Surgical skin markers by Scanlan International Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin marking pen, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8a70ec9e-895e-4f14-b6b2-ed0912b1ef63 35 fields · synced May 30, 2026