VERIFY RESI-TEST SLIDE-THRU

Primary DI
10724995231931
Brand
VERIFY RESI-TEST SLIDE-THRU
Company
STERIS CORPORATION
Model
Resi-Test
Catalog number
2D79QH
Device description
VERIFY RESI-TEST SLIDE-THRU Brush -2.6-5.0mm, 290cm length is designed to detect a broad spectrum of protein residues and is intended for use after manual or automated cleaning and prior to high level disinfection or sterilization.
Published
2025-04-10
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
SDCQualitative cleaning process protein indicator

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
SDCQualitative Cleaning Process Protein IndicatorGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
DEN230085000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
DEN230085000VERIFY RESI-TEST SLIDE-THRU Cleaning Process Protein (CPP) IndicatorSteris2024-11-12SDC

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10724995231931PackageGS125In Commercial Distribution
50724995231939PackageGS14In Commercial Distribution
00724995231934PrimaryGS10
00724995002305Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1072499523193110724995231931
5072499523193950724995231939
00724995231934007249952319347249952319340724995231934
00724995002305007249950023057249950023050724995002305

GMDN Terms#

Term, Definition table
TermDefinition
Surgical instrument/endoscope cleaning utensil, single-useA non-absorbent, non-powered, hand-held device in the form of a brush, a wire, strip of metal, or handle intended to clean the exterior and/or interior (lumen) of a surgical instrument (e.g., bur, reamer, bone tap, suturing device, sheath/shaft, ultrasonic surgical handpiece) and/or endoscope. The bristles, fibres or spines of brushes may be mounted along a single plane or radiate out around a central shaft, and may be soft or stiff; the shaft/handle of brushes may be flexible or rigid. The device may be used to clean endoscopic or open-surgery instruments, and it may have a handle or a connector/adaptor at the proximal end. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)548-4873xx@xx.xx

Regulatory Flags#

DUNS number
961394798
Device count
25
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10724995231900VERIFY RESI-TEST SLIDE-THRUSTERIS CORPORATIONSDC2025-04-10
00724995231910VERIFY RESI-TEST SLIDE-THRUSTERIS CORPORATIONSDC2025-04-10
00724995231927VERIFY RESI-TEST SLIDE-THRUSTERIS CORPORATIONSDC2025-04-10
00724995231934VERIFY RESI-TEST SLIDE-THRUSTERIS CORPORATIONSDC2025-04-10
10724995231917VERIFY RESI-TEST SLIDE-THRUSTERIS CORPORATIONSDC2025-04-10
10724995231924VERIFY RESI-TEST SLIDE-THRUSTERIS CORPORATIONSDC2025-04-10
00724995231903VERIFY RESI-TEST SLIDE-THRUSTERIS CORPORATIONSDC2025-04-10