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Aquastat SFR

FDA UDI

Class II (US FDA UDI)

by Mrp, Llc

Identity

Trade Name
Aquastat SFR FDA UDI
Generic Name
Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial FDA UDI
Device Name
Pre-filled Flush syringe with 0.9% NaCL (saline), 20mL, Sterile Field Ready FDA UDI
Model / Reference
2S0708 FDA UDI
Description
Pre-filled Flush syringe with 0.9% NaCL (saline), 20mL, Sterile Field Ready FDA UDI

Identifiers

Catalog Number
2S0708 FDA UDI
Primary DI / UDI-DI
10859809005047 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

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

Aquastat SFR by Mrp, Llc — 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
Mrp, Llc

Sources (1)

  • FDA UDI 18a5c631-c6b7-450d-8aea-b4c26f022f3c 37 fields · synced Jun 1, 2026