FDA.reportPublic FDA data

Dukal

Primary DI
20665973027184
Brand
Dukal
Company
DUKAL CORPORATION
Model
27305
Catalog number
27305
Device description
Sterilization Pouch, 3.5" x 10" NS
Published
2022-03-30
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
FRGWrap, sterilization

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FRGWrap, SterilizationGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K162258000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K162258000Self Sealing Sterilization PouchesTianchang Jiarui Packaging Material Co., Ltd.2017-04-28FRG

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20665973027184PackageGS14In Commercial Distribution
10665973027187PrimaryGS10
00665973027173Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2066597302718420665973027184
1066597302718710665973027187
00665973027173006659730271736659730271730665973027173

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

Contacts#

Phone, Email table
PhoneEmail
+1(631)656-3800kmckigney@dukal.com

Regulatory Flags#

DUNS number
791014871
Device count
500
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
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
20665973027146Dukal27301273012022-03-30
20665973027153Dukal27302273022022-03-30
20665973027160Dukal27303273032022-03-30
20665973027177Dukal27304273042022-03-30
20665973027191Dukal27306273062022-03-30
20665973027207Dukal27307273072022-03-30
20665973028891Dukal158015802022-03-30
00665973027173Dukal27304-BK27304-BK2022-03-30
20665973028099DukalAB100AB1002022-03-28
60665973010375DukalCM-101CM-1012020-10-14
20665973004970Dukal154015402016-09-24
20665973004987Dukal155015502016-09-24
20665973004994Dukal156015602016-09-24
20665973005557Dukal154115412016-09-24
20665973005564Dukal154215422016-09-24
20665973017765Derma Science17240172402016-12-02
30665973027112Capseus SurgicalBDC-15BDC-152019-10-23
20665973016775Tech-Med601260122016-09-24
20665973016782Tech-Med601060102016-09-24
20665973016799Tech-Med6010-T6010-T2016-09-24

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00840456201312JMUJMU DENTAL, INCFRG2026-06-05
00840456201831JMUJMU DENTAL, INCFRG2026-06-05
00840456201848JMUJMU DENTAL, INCFRG2026-06-05
00840456201855JMUJMU DENTAL, INCFRG2026-06-05
00840456201862JMUJMU DENTAL, INCFRG2026-06-05
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00840456215203JMUJMU DENTAL, INCFRG2026-06-05
00840456216804JMUJMU DENTAL, INCFRG2026-06-05
00840456216811JMUJMU DENTAL, INCFRG2026-06-05
00840456216828JMUJMU DENTAL, INCFRG2026-06-05