← Back to catalogue

McKesson

FDA UDI

Class II (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Vascular catheter/cannula flush solution, non-anticoagulant, non-antimicrobial FDA UDI
Device Name
Prefilled Flush Syringe NORMAL SALINE , IV FLUSH 10ML FILL/10ML SYRINGE FDA UDI
Model / Reference
16-SFS1010 FDA UDI
Description
Prefilled Flush Syringe NORMAL SALINE , IV FLUSH 10ML FILL/10ML SYRINGE FDA UDI

Identifiers

Primary DI / UDI-DI
10612479273143 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

No

FDA UDI

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

McKesson by Mckesson Medical-Surgical Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 69e86ce3-e0fa-4492-b236-0572ef17e67e 34 fields · synced May 31, 2026