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PremierPro

FDA UDI

Class II (US FDA UDI)

by Svs Llc

Identity

Trade Name
PremierPro FDA UDI
Generic Name
Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial FDA UDI
Device Name
Pre-filled Normal Saline Flush Syringe, 10mL Fill 0.9% Sodium Chloride Injection, Sterile Fluid Pathway FDA UDI
Model / Reference
FL1010D FDA UDI
Description
Pre-filled Normal Saline Flush Syringe, 10mL Fill 0.9% Sodium Chloride Injection, Sterile Fluid Pathway FDA UDI

Identifiers

Catalog Number
FL1010D FDA UDI
Primary DI / UDI-DI
00811220035068 FDA UDI
510(k) Number
K220060 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

Yes

FDA UDI

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

PremierPro by Svs 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Svs Llc

Sources (1)

  • FDA UDI 5a6677d3-01b6-49f8-b84d-d7bed1668f82 37 fields · synced Jun 1, 2026