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Aseptic Fluid Transfer Set

FDA UDI

Class II (US FDA UDI)

by Mentor Texas LP

Identity

Trade Name
Aseptic Fluid Transfer Set FDA UDI
Generic Name
Fluid transfer set, general-purpose FDA UDI
Device Name
Aseptic Fluid Transfer Set FDA UDI
Model / Reference
350-8400 FDA UDI
Description
Aseptic Fluid Transfer Set FDA UDI

Identifiers

Catalog Number
350-8400 FDA UDI
Primary DI / UDI-DI
00081317024941 FDA UDI
510(k) Number
K780417 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Fluid transfer set, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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: Fluid transfer set, general-purpose

Aseptic Fluid Transfer Set by Mentor Texas LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluid transfer set, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mentor Texas LP

Sources (1)

  • FDA UDI 40ddf44d-9014-48f5-b120-bdc5145a6196 36 fields · synced May 30, 2026