FDA.reportPublic FDA data

Steriking®

Primary DI
06438263662026
Brand
Steriking®
Company
WIPAK PACKAGING (CHANGSHU) CO., LTD.
Model
SS2
Catalog number
SS2
Device description
Single use sterilization packaging
Published
2016-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

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
K953776000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K953776000STERIKING STERILIZATION POUCHES & ROLLSWihuri OY1995-10-12KCT

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
06438263662026PackageGS15In Commercial Distribution
06438263660411PrimaryGS10
06438263663221Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
06438263662026064382636620266438263662026
06438263660411064382636604116438263660411
06438263663221064382636632216438263663221

GMDN Terms#

Term, Definition table
TermDefinition
Sterilization packaging, single-useA device, typically in the form of a paper sheet, envelope, bag, wrap, or similar, intended to be used to contain medical devices that are to be sterilized. It is designed to allow sterilization of the enclosed medical device and also to maintain sterility of the device until the packaging is opened for use of the device, or until a predetermined shelf date is expired. This is a single-use device.

Sterilization Methods#

Method table
Method
Ethylene Oxide;Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
543001936
Device count
200
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
true
Donation ID number
false
Contains natural rubber latex
true
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06438263660114Steriking®LTSS5ALTSS5A2016-09-26
06438263660138Steriking®LTSS4LTSS42016-09-26
06438263660367Steriking®SS6SS62016-09-23
06438263660381Steriking®SS5ASS5A2016-09-23
06438263660398Steriking®SS4ASS4A2016-09-23
06438263660404Steriking®SS4SS42016-09-23
06438263660411Steriking®SS2SS22016-09-23
06438263660428Steriking®SS1SS12016-09-23
06438263660435Steriking®SS10SS102016-09-23
06438263660534Steriking®SS3SS32016-09-23
06438263660657Steriking®LTS7520LTS7520Y2016-09-26
06438263660664Steriking®LTS2550LTS2550Y2016-09-26
06438263660671Steriking®LTS2538LTS2538Y2016-09-26
06438263660688Steriking®LTS2038LTS2038Y2016-09-26
06438263660695Steriking®LTS1530LTS1530Y2016-09-26
06438263660701Steriking®LTS1025LTS1025Y2016-09-26
06438263660107Steriking®LTSS7LTSS72016-09-26
06438263663078Steriking®LTSS5ALTSS5A2016-09-26
06438263660121Steriking®LTSS4ALTSS4A2016-09-26
06438263663092Steriking®LTSS4LTSS42016-09-26

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Primary DI, Brand, Company table
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00385640092401INSTRUSAFESummit Medical, Inc.KCT2026-08-07
00385640092418INSTRUSAFESummit Medical, Inc.KCT2026-08-07
00385640092425INSTRUSAFESummit Medical, Inc.KCT2026-08-07
00385640092432INSTRUSAFESummit Medical, Inc.KCT2026-08-07
00385640092449INSTRUSAFESummit Medical, Inc.KCT2026-08-07
00385640092456INSTRUSAFESummit Medical, Inc.KCT2026-08-07