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Excelsior

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Excelsior FDA UDI
Generic Name
Vascular catheter flush syringe FDA UDI
Device Name
0.9% Sodium Chloride Injection, USP FDA UDI
Model / Reference
17011 FDA UDI
Description
0.9% Sodium Chloride Injection, USP FDA UDI

Identifiers

Catalog Number
17011 FDA UDI
Primary DI / UDI-DI
10363807170114 FDA UDI
FDA Product Code
NGT FDA UDI
GMDN Term
Vascular catheter flush syringe 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

No

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 — 10 Milliliter FDA UDI

Category: Vascular catheter flush syringe

Excelsior by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter flush syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI e5fe4d2b-7edb-46f9-a9f6-661ec4c211e2 37 fields · synced May 31, 2026