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EXEL 2-3mL SYR ONLY L-L

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 26200

by Exelint International, Co.

Identity

Trade Name
EXEL 2-3mL SYR ONLY L-L EUDAMED
EXEL Disposable Syringe, 3mL Luer Lock Tip EUDAMED
EXEL Syringes FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
Syringe only EUDAMED
EXEL Disposable Syringe EUDAMED
Syringe, 3CC, Luer Lock with cap FDA UDI
Model / Reference
26200 EUDAMEDFDA UDI
Description
Syringe, 3CC, Luer Lock with cap FDA UDI

Identifiers

Catalog Number
26200 FDA UDI
Primary DI / UDI-DI
00020221262001 EUDAMEDFDA UDI
Basic UDI-DI
B-00020221262001 EUDAMED
20221SYRONLY263ES EUDAMED
FDA Product Code
FMF FDA UDI
EMDN Code
A020199 SYRINGES, SINGLE-USE - OTHER EUDAMED
A020102020102 INFUSION AND IRRIGATION SYRINGES, LUER LOCK CONE, 3-PIECE WITHOUT NEEDLE, SINGLE-USE EUDAMED
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class I 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

No

EUDAMEDEUDAMED

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 ONLY L-L by Exelint International, Co. — Class I — 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

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Manufacturer

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

Sources (3)

  • EUDAMED 02253658-0bde-4ff2-a21b-99f9b4b5ca50 61 fields · synced Jun 18, 2026
  • FDA UDI e2d600d7-6801-4be5-9b45-6f721067f1ad 34 fields · synced May 30, 2026
  • EUDAMED 6c8be6a0-04a6-4afc-919f-75e2d5ba09a7 61 fields · synced Jun 18, 2026