← Back to catalogue

SuperDART® ONE PASS™ Validated Channel Cleaning Device

FDA UDI

Class I (US FDA UDI)

by Primed Instruments Inc

Identity

Trade Name
SuperDART® ONE PASS™ Validated Channel Cleaning Device FDA UDI
Generic Name
Surgical instrument/endoscope cleaning utensil, single-use FDA UDI
Device Name
BRUSH CLEANING 3 TO 4.5MM X 85CM MULTI ACTION PULL THROUGH SQUEEGEE. HIBC/UPN: M45392332 FDA UDI
Model / Reference
9233 FDA UDI
Description
BRUSH CLEANING 3 TO 4.5MM X 85CM MULTI ACTION PULL THROUGH SQUEEGEE. HIBC/UPN: M45392332 FDA UDI

Identifiers

Catalog Number
9233-25 FDA UDI
Primary DI / UDI-DI
00666416121335 FDA UDI
FDA Product Code
MNL FDA UDI
GMDN Term
Surgical instrument/endoscope cleaning utensil, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Surgical instrument/endoscope cleaning utensil, single-use

SuperDART® ONE PASS™ Validated Channel Cleaning Device by Primed Instruments Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/endoscope cleaning utensil, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI c78a92f6-34ee-4bd7-ab93-79eccfaaf5e5 37 fields · synced Jun 8, 2026