← Back to catalogue

Trackable Intra Uterine Insemination Catheter Open Tip

FDA UDI

Class II (US FDA UDI)

by Allwin Medical Devices, Inc.

Identity

Trade Name
Trackable Intra Uterine Insemination Catheter Open Tip FDA UDI
Generic Name
Assisted reproduction transfer catheter/set FDA UDI
Model / Reference
Trackable Open Tip FDA UDI

Identifiers

Catalog Number
T-IUI-O FDA UDI
Primary DI / UDI-DI
00819374022019 FDA UDI
510(k) Number
K190522 FDA UDI
FDA Product Code
MFD FDA UDI
GMDN Term
Assisted reproduction transfer catheter/set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5250 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: Assisted reproduction transfer catheter/set

Trackable Intra Uterine Insemination Catheter Open Tip by Allwin Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction transfer catheter/set.

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 e947ee7a-1d16-4944-b47a-4cb1fbff4fc9 35 fields · synced May 30, 2026