Artman Instrumens

FDA UDI

Class II (US FDA UDI)

by Wise Linkers Llc

Identity

Trade Name: Artman Instrumens FDA UDI
Generic Name: Medication cartridge syringe, safety-needle FDA UDI
Device Name: Dental 2.5 Ring Aspirating Syringe 1.8ml Set of 3 ARTMAN FDA UDI
Model / Reference: S4CY6MD8M5 FDA UDI
Description: Dental 2.5 Ring Aspirating Syringe 1.8ml Set of 3 ARTMAN FDA UDI

Identifiers

Catalog Number: 1 FDA UDI
Primary DI / UDI-DI: D127S4CY6MD8M51 FDA UDI
FDA Product Code: EJI FDA UDI
GMDN Term: Medication cartridge syringe, safety-needle FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.6770 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Medication cartridge syringe, safety-needle

Artman Instrumens by Wise Linkers Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medication cartridge syringe, safety-needle.

Medline — MEDLINE INDUSTRIES, INC. · Class II
Doctors Choice — Supply Line International Medical, LLC · Class II
Doctors Choice — Supply Line International Medical, LLC · Class II
Doctors Choice — Supply Line International Medical, LLC · Class II
Medline — MEDLINE INDUSTRIES, INC. · Class II
NEEDLES 25x1 — GERI-GENTLE CORPORATION · Class II
Doctors Choice — Supply Line International Medical, LLC · Class II
Doctors Choice — Supply Line International Medical, LLC · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Wise Linkers Llc

Sources (1)

FDA UDI 903f4c7c-9174-44ca-9689-235798608202 34 fields · synced May 30, 2026