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Alleset

FDA UDI

Class I (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
Alleset FDA UDI
Generic Name
Skin marking pen, single-use FDA UDI
Device Name
Skin Marker_Standard Tip with Ruler and Labels_sterile_100EA/CS FDA UDI
Model / Reference
25-S003-S FDA UDI
Description
Skin Marker_Standard Tip with Ruler and Labels_sterile_100EA/CS FDA UDI

Identifiers

Primary DI / UDI-DI
16931918166469 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

No

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

Alleset by GRI Medical & Electronic Technology Co., Ltd. — 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 85622011-45aa-41ee-b393-cb45cc725c5d 34 fields · synced Sep 18, 2026