V. Mueller

Primary DI
00724995243319
Brand
V. Mueller
Company
Steris Corporation
Model
TB312
Catalog number
TB312
Device description
GENESIS BASKET ID TAG EXTRA LARGE, FUCHSIA 1 X 3 inches 2.54 X 7.6CM
Published
2026-10-15
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
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
KCTSterilization wrap containers, trays, cassettes & other accessories

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KCTSterilization Wrap Containers, Trays, Cassettes & Other AccessoriesGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K142529000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K142529000Genesis Reusable Rigid Container SystemCarefusion 2200, Inc.2015-01-08KCT

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10885403185472PreviousGS10
00724995243319PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1088540318547210885403185472
00724995243319007249952433197249952433190724995243319

GMDN Terms#

Term, Definition table
TermDefinition
Device operating status label/tag, reusableA label or a tag intended to indicate the operating/calibration status (e.g., calibrated, repair required, out of service) and/or sterility record of the device to which it is attached; it does not include any additional functionality and does not include a sterilization process indicator. It is typically constructed from a durable material and may be designed to a specific standard. This is a reusable device.

Contacts#

Phone, Email table
PhoneEmail
+1(800)548-5873xx@xx.xx

Regulatory Flags#

DUNS number
149891242
Device count
1
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
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00724995023911VERIFYIncubatorS30802021-03-31
00724995023928VERIFYIncubatorS30812021-03-31
00724995023935VERIFYIncubatorS30822021-03-31
00724995095659VERIFYIncubatorS32712021-03-31
00724995301934V. MuellerNL1060NL10602026-10-21
00724995301958V. MuellerNL1064NL10642026-10-21
00724995301972V. MuellerNL1073NL10732026-10-21
00724995301989V. MuellerNL1074NL10742026-10-21
00724995301996V. MuellerNL1075NL10752026-10-21
00724995326906V. MuellerRH1045RH10452026-10-21
00724995239909V. MuellerDP11DP112026-10-15
00724995239916V. MuellerDP12DP122026-10-15
00724995239923V. MuellerDP13DP132026-10-15
00724995239930V. MuellerDP14DP142026-10-15
00724995239947V. MuellerDP15DP152026-10-15
00724995239985V. MuellerED112ED1122026-10-15
00724995239992V. MuellerED15ED152026-10-15
00724995240004V. MuellerED16ED162026-10-15
00724995240011V. MuellerED17ED172026-10-15
00724995240028V. MuellerED19ED192026-10-15

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