EcoFLX™ Empty Mixing Container

Primary DI
10816415020512
Brand
EcoFLX™ Empty Mixing Container
Company
DOUGLAS MEDICAL PRODUCTS, INC.
Model
DME5000
Device description
EcoFLX 5000mL Empty IV Mixing Container (EVA)
Published
2018-05-06
Public version status
Update
Distribution status
Not 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
KPEContainer, I.V.

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KPEContainer, I.V.General Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K932640000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K932640000EVA EMPTY MIXING CONTAINERDouglas Medical Products Corp.1993-11-10KPE

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10816415020512PrimaryGS10
00816415020515Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1081641502051210816415020512
00816415020515008164150205158164150205150816415020515

GMDN Terms#

Term, Definition table
TermDefinition
Intravenous administration bag/bottleAn empty pouch or bottle made of plastic or glass intended to contain a fluid (e.g., saline, medication) for intravenous (IV) administration; some types may in addition be intended for enteral feeding applications. It may be composed of one or more chambers and might be provided with a short length of tubing; however, it does not include other associated items (e.g., clamp, spike) [i.e., not an IV administration set] and is not intended to be directly connected to the IV catheter. This is a single-use device.

Regulatory Flags#

DUNS number
121040922
Device count
40
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
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
10816415020079Kew MedicalQEG61142017-09-15
10816415020086Kew MedicalQEG61152017-09-15
10816415020093Kew MedicalQEG61332017-09-15
10816415020109Kew MedicalQEG61322017-09-15
10816415020116Kew MedicalQEG62112017-09-15
10816415020123Kew MedicalQEG62102017-09-15
10816415020130Kew MedicalQEG63112017-09-15
10816415020147Kew MedicalQEG63102017-09-15
10816415020246Kew MedicalQEG41702017-09-15
10816415020000Lune MedicalG4100002017-09-15
10816415020017Lune MedicalG4101002017-09-15
10816415020024Lune MedicalG4102002017-09-15
10816415020031Kew MedicalQAP31022017-09-15
10816415020048Kew MedicalQAP51282017-09-15
10816415020055Kew MedicalQAP31222017-09-15
10816415020154Kew MedicalQAU91022017-09-15
10816415020161Kew MedicalQAU91222017-09-15
10816415020178Kew MedicalQAU51282017-09-15
10816415020185Kew MedicalQAU91952017-09-15
10816415020192Kew MedicalQAU51312017-09-15

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Primary DI, Brand, Company table
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00075289522239ISO-MEDTRANZONIC COMPANIES, THEKPE2026-06-22
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00075289522253ISO-MEDTRANZONIC COMPANIES, THEKPE2026-06-10
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