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SuperDART® ONE PASS™ ECCD

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9253-25

by PriMed Instruments Inc.

Identity

Trade Name
SuperDART® ONE PASS™ ECCD EUDAMED
SuperDART® ONE PASS™ Validated Channel Cleaning Device FDA UDI
Generic Name
Surgical instrument/endoscope cleaning utensil, single-use FDA UDI
Device Name
Disposable Cleaning Brushes for Flexible Endoscopes Reprocessing EUDAMED
BRUSH CLEANING 3 TO 4.5MM X 122CM MULTI ACTION PULL THROUGH SQUEEGEE. HIBC/UPN: M45392532 FDA UDI
Model / Reference
9253-25 EUDAMED
9253 FDA UDI
Description
BRUSH CLEANING 3 TO 4.5MM X 122CM MULTI ACTION PULL THROUGH SQUEEGEE. HIBC/UPN: M45392532 FDA UDI

Identifiers

Catalog Number
9253-25 FDA UDI
Primary DI / UDI-DI
00666416121144 EUDAMEDFDA UDI
Basic UDI-DI
666416DCBWT EUDAMED
Secondary DI
M45392532 EUDAMED
Unit of Use DI
00666416121137 EUDAMED
FDA Product Code
MNL FDA UDI
EMDN Code
V070102 DIGESTIVE ENDOSCOPY ENDOSCOPES CLEANING BRUSHES EUDAMED
GMDN Term
Surgical instrument/endoscope cleaning utensil, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
876.1500 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

EUDAMED

Measuring Function

No

EUDAMED

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

SuperDART® ONE PASS™ ECCD by Primed Instruments Inc — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
CA-MF-000002760
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED b7d884ad-5ef8-494a-9061-e8e0fe6a70a0 61 fields · synced Jun 18, 2026
  • FDA UDI 0bbfd4f4-4ac4-47d0-8b34-b8f76d0ad08b 37 fields · synced May 30, 2026