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EXEL 2-3mL SYR W/ SAFETY NDL 23GX5/8"

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 27118

by Exelint International, Co.

Identity

Trade Name
EXEL 2-3mL SYR W/ SAFETY NDL 23GX5/8" EUDAMED
EXEL 2-3mL SYR W/ SAFETY NDL 23GX5/8" L-L FDA UDI
Generic Name
General-purpose syringe/needle FDA UDI
Device Name
Syringe with safety needle EUDAMED
EXEL 2-3mL SYR W/ SAFETY NDL 23GX5/8" L-L, 50/BX, 8BX/CS, 400PC/CS FDA UDI
Model / Reference
27118 EUDAMEDFDA UDI
Description
EXEL 2-3mL SYR W/ SAFETY NDL 23GX5/8" L-L, 50/BX, 8BX/CS, 400PC/CS FDA UDI

Identifiers

Catalog Number
27118 FDA UDI
Primary DI / UDI-DI
00020221271188 EUDAMEDFDA UDI
Basic UDI-DI
B-00020221271188 EUDAMED
FDA Product Code
MEG FDA UDI
EMDN Code
A0101010101 HYPODERMIC SYRINGE NEEDLES, WITH SAFETY SYSTEMS EUDAMED
GMDN Term
General-purpose syringe/needle FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hypodermic needle, single-use

EXEL 2-3mL SYR W/ SAFETY NDL 23GX5/8" by Exelint International, Co. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hypodermic needle, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000037396
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED b1dcbcbc-9fc3-4b33-afe5-86f53e0ed298 61 fields · synced Jun 18, 2026
  • FDA UDI 574665a6-583b-42b9-9ad6-9dc23065274c 35 fields · synced May 30, 2026