FDA.reportPublic FDA data

ECLIPSE

Primary DI
16935550817024
Brand
ECLIPSE
Company
Jiangsu Shenli Medical Production Co.,Ltd.
Model
PRPB-368652
Device description
Eclipse Blood Collection Set SIZE:21G/19.5mm
Published
2022-03-11
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
FMINeedle, Hypodermic, Single Lumen

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FMINeedle, Hypodermic, Single LumenGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K163093000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K163093000Safety Blood Collection SetJiangsu Shenli Medical Production Co., Ltd.2017-03-14FMI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
16935550817024PackageGS150In Commercial Distribution
26935550817021PackageGS112In Commercial Distribution
06935550817027PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1693555081702416935550817024
2693555081702126935550817021
06935550817027069355508170276935550817027

GMDN Terms#

Term, Definition table
TermDefinition
Blood collection set, invasiveA collection of devices intended to be used by a healthcare professional, in combination with evacuated blood collection tubes, for the routine collection of multiple blood specimens from a patient, via one venipuncture, for clinical analyses. It consists of a blood collection needle or venous butterfly/scalp vein needle and additional devices that may include tubing, male/female Luer-lock connectors, clamps, and a blood collection tube holder. Blood access is directly through the vein with the needle. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
420611311
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
true
Expiration date on label
true
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
06935550817010BDS21G×3/4‘’2022-01-26
06935550817027ECLIPSEPRPB-3686522022-03-11
06935550810035Tianzi1ml2021-08-02
06935550810103ECLIPSEPRP2600-10ML2022-03-11
06935550810110Tianzi20ML2020-12-05
06935550813012Tianzi10ml2020-12-05
06935550810028NA1ml 2021-02-28
06935550810059DPS3ml2020-12-17
06935550810011DPS1ml2020-11-27
16935550810094NORTH AMERICAN RESCUEZZ-0070ZZ-00702018-09-22
06935550812015Tianzi1ml Luer Slip 25G×1‘’01LS252023-02-28
06935550812312Tianzi3ml Luer Lock 23G×1‘’03LL232023-02-28
16935550812012Tianzi1ml Luer Slip 25G×1‘’01LS252023-02-28
16935550812319Tianzi3ml Luer Lock 23G×1‘’03LL232023-02-28
16935550810100ECLIPSEPRP2600-10ML2022-03-11
16935550817017BDS21G×3/4‘’2022-01-26
16935550810032Tianzi1ml2021-08-02
06935550812022NA3ml 21G×1''2021-02-28
06935550811025NA23G×1''2021-02-28
16935550812029NA3ml 21G×1''2021-02-28

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