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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Skin marking guide, single-use FDA UDI
Device Name
MARKER,SKIN,W/RULER,DUAL,STOP FDA UDI
Model / Reference
DYNJSMD01GS FDA UDI
Description
MARKER,SKIN,W/RULER,DUAL,STOP FDA UDI

Identifiers

Catalog Number
DYNJSMD01GS FDA UDI
Primary DI / UDI-DI
10884389361948 FDA UDI
FDA Product Code
FZZ FDA UDI
GMDN Term
Skin marking guide, 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

Yes

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 guide, single-use

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin marking guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f71b655b-71a8-4fd7-ab32-6464218f0e1b 35 fields · synced May 30, 2026