← Back to catalogue

EXEL 20-25mL AMBER SYR ONLY L-S W/ TIP CAP

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 26288

by Exelint International, Co.

Identity

Trade Name
EXEL 20-25mL AMBER SYR ONLY L-S W/ TIP CAP EUDAMEDFDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
Syringe only EUDAMED
EXEL 20-25mL AMBER SYR ONLY L-S W/ TIP CAP, 50/BX, 500/CS FDA UDI
Model / Reference
26288 EUDAMEDFDA UDI
Description
EXEL 20-25mL AMBER SYR ONLY L-S W/ TIP CAP, 50/BX, 500/CS FDA UDI

Identifiers

Catalog Number
26288 FDA UDI
Primary DI / UDI-DI
00020221262889 EUDAMEDFDA UDI
Basic UDI-DI
B-00020221262889 EUDAMED
510(k) Number
K861153 FDA UDI
FDA Product Code
FMF FDA UDI
EMDN Code
W01029004 COATED TUBES AND BEADS (UNASSIGNABLE) (IC) 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
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

No

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

EXEL 20-25mL AMBER SYR ONLY L-S W/ TIP CAP by Exelint International, Co. — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

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 (2)

  • EUDAMED ca1f7593-5c85-46a0-a601-bc10d8b404fb 61 fields · synced Jun 19, 2026
  • FDA UDI 1e6215e0-bd39-4340-bb0c-361206d33228 36 fields · synced May 27, 2026