← Back to catalogue

EXEL 2-3mL SYR 22GX3/4"

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 26601

by Exelint International, Co.

Identity

Trade Name
EXEL 2-3mL SYR 22GX3/4" EUDAMED
EXEL Disposable Syringe with Needle, 3mL Luer Slip Tip W/ 22G x 3/4" EUDAMED
EXEL Syringes FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
Syringe with needle EUDAMED
EXEL Disposable Syringe with Needle EUDAMED
Syringe, 3CC, Luer Slip, 22G x 3/4 FDA UDI
Model / Reference
26601 EUDAMEDFDA UDI
Description
Syringe, 3CC, Luer Slip, 22G x 3/4 FDA UDI

Identifiers

Catalog Number
26601 FDA UDI
Primary DI / UDI-DI
00020221266016 EUDAMEDFDA UDI
Basic UDI-DI
B-00020221266016 EUDAMED
20221SYRNDL261PG EUDAMED
FDA Product Code
FMF FDA UDI
EMDN Code
A0101010102 HYPODERMIC SYRINGE NEEDLES, W/O SAFETY SYSTEMS EUDAMED
A020102010201 INFUSION AND IRRIGATION SYRINGES, LUER CONE, 3-PIECE WITH NEEDLE, SINGLE-USE EUDAMED
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
Market of Registration
Netherlands EUDAMED
Austria 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMEDEUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

EXEL 2-3mL SYR 22GX3/4" by Exelint International, Co. — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

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

Sources (3)

  • EUDAMED 356aead9-5482-4908-afcf-e5544a3ef9a7 61 fields · synced Jun 19, 2026
  • FDA UDI 86f46853-39cb-4233-953a-c1bbcb5f9f59 34 fields · synced May 30, 2026
  • EUDAMED 7f462491-22ca-4cee-b29a-47574c84cbea 61 fields · synced Jun 19, 2026