← Back to catalogue

Advect

FDA UDI

Class II (US FDA UDI)

by Charter Medical, Llc

Identity

Trade Name
Advect FDA UDI
Generic Name
Fluid transfer set, general-purpose FDA UDI
Device Name
Fluid Transfer Sets 6" PVC with Spike and Male Luer FDA UDI
Model / Reference
CT-018-94 FDA UDI
Description
Fluid Transfer Sets 6" PVC with Spike and Male Luer FDA UDI

Identifiers

Catalog Number
CT-018-94 FDA UDI
Primary DI / UDI-DI
00817827026218 FDA UDI
FDA Product Code
KSB FDA UDI
GMDN Term
Fluid transfer set, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9875 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: Fluid transfer set, general-purpose

Advect by Charter Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluid transfer set, general-purpose.

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 62bae88d-2d52-47dc-95f2-66ccd2f62b1b 36 fields · synced May 31, 2026