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Praxiject™ 0.9% NaCl

FDA UDI

Class II (US FDA UDI)

by MedXL

Identity

Trade Name
Praxiject™ 0.9% NaCl FDA UDI
Generic Name
Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial FDA UDI
Device Name
20 mL of 0.9% Sodium Chloride Injection USP in a 20 mL syringe FDA UDI
Model / Reference
3706US FDA UDI
Description
20 mL of 0.9% Sodium Chloride Injection USP in a 20 mL syringe FDA UDI

Identifiers

Catalog Number
3706US FDA UDI
Primary DI / UDI-DI
10682686004762 FDA UDI
510(k) Number
K231754 FDA UDI
FDA Product Code
NGT FDA UDI
GMDN Term
Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 20 Milliliter FDA UDI

Category: Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial

Praxiject™ 0.9% NaCl by MedXL — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MedXL

Sources (1)

  • FDA UDI 9c6852e0-18a7-4ee8-9ad2-15b58d698cc2 38 fields · synced May 31, 2026