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EXEL 10-12mL SYR 22GX1"

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 26250

by Exelint International, Co.

Identity

Trade Name
EXEL 10-12mL SYR 22GX1" EUDAMED
EXEL Disposable Syringe with Needle, 10mL Luer Lock Tip W/ 22G x 1” 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, 10CC, Luer Lock, 22G X 1 FDA UDI
Model / Reference
26250 EUDAMEDFDA UDI
Description
Syringe, 10CC, Luer Lock, 22G X 1 FDA UDI

Identifiers

Catalog Number
26250 FDA UDI
Primary DI / UDI-DI
00020221262506 EUDAMEDFDA UDI
Basic UDI-DI
B-00020221262506 EUDAMED
20221SYRNDL261PG EUDAMED
FDA Product Code
FMF FDA UDI
EMDN Code
A0101010102 HYPODERMIC SYRINGE NEEDLES, W/O SAFETY SYSTEMS EUDAMED
A020102020101 INFUSION AND IRRIGATION SYRINGES, LUER LOCK 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 10-12mL SYR 22GX1" 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

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Manufacturer

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

Sources (3)

  • EUDAMED fe7dfb86-20ac-4d0d-84b9-dfb7fababeed 61 fields · synced Jul 30, 2026
  • FDA UDI faf5737b-d344-4176-8232-0523b58a5bd1 34 fields · synced May 30, 2026
  • EUDAMED 7df1c03d-83dd-4422-8769-3e2e4335ab1c 61 fields · synced Jul 30, 2026