RxCrush

Primary DI
30850006611172
Brand
RxCrush
Company
RESOLVE DESIGNS LLC
Model
EC06-50
Catalog number
EC06
Device description
Female ENFit to Female Catheter Adapter - Push-on. Connects male ENFit (e.g. RxCrush Pouch) to male Catheter syringe.
Published
2024-12-17
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
KYXDispenser, Liquid Medication

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KYXDispenser, Liquid MedicationGeneral Hospital1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10850006611178PackageGS15In Commercial Distribution
30850006611172PackageGS11000In Commercial Distribution
00850006611171PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1085000661117810850006611178
3085000661117230850006611172
00850006611171008500066111718500066111710850006611171

GMDN Terms#

Term, Definition table
TermDefinition
ENFit/non-ISO80369-standardized linear connectorA small, non-powered, noninvasive, tubular two-way/linear connector with an ENFit connection (designed according to ISO 80369-3 for enteral applications) at one end and a connection which is not designed according to ISO 80369 at the other end (typically barbed, conical, ENLock, threaded or non-Luer-slip), intended to connect an enteral device (e.g., enteral syringe, feeding tube, administration set) with an ENFit connection typically with tubing or syringe; it does not connect a vial/bottle (i.e., not a vial/bottle adaptor). It does not have a Luer connection(s) (neither lock nor slip), and does not incorporate a filter, valve, clamp nor tubing. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Keep out of sunlight. Keep out of moisture.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
877.343.2783info@rxcrush.com

Regulatory Flags#

DUNS number
091290281
Device count
1
DM exempt
false
Premarket exempt
true
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
00850006611867RxCrushCA04-100CA042025-04-30
30850006611868RxCrushCA04-100CA042025-04-30
00850006611010RxCrushPP06-50PP062024-12-17
00850006611027RxCrushEO05-100EO052024-12-17
00850006611034RxCrushPC11-ENPC112024-12-17
00850006611058RxCrushCA03-100CA032024-12-17
00850006611096RxCrushPP20-100PP202024-12-17
00850006611102RxCrushCA02-100CA022024-12-17
00850006611126RxCrushEL02-100EL022024-12-17
00850006611140RxCrushEO02-100EO022024-12-17
00850006611157RxCrushET01-100ET012024-12-17
00850006611164RxCrushPP10-50PP102024-12-17
00850006611171RxCrushEC06-50EC062024-12-17
00850006611195RxCrushPP08-50PP082024-12-17
00850006611256RxCrushPC11-REFPC112024-12-17
00850006611263RxCrushPC11-SPPC112024-12-17
00850006611300RxCrushPC11-FRPC112024-12-17
00850006611836RxCrushPC16-1PC162024-12-17
00850006611843RxCrushPP11-5PP112024-12-17
00850006611850RxCrushPP142024-12-17

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