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VitaVitro

FDA UDI

Class II (US FDA UDI)

by Shenzhen Vitavitro Bio-Tech Co., Ltd.

Identity

Trade Name
VitaVitro FDA UDI
Generic Name
Assisted reproduction transfer catheter/set FDA UDI
Model / Reference
ET-S FDA UDI

Identifiers

Primary DI / UDI-DI
06971982050335 FDA UDI
510(k) Number
K240307 FDA UDI
FDA Product Code
MQF FDA UDI
GMDN Term
Assisted reproduction transfer catheter/set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6110 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assisted reproduction transfer catheter/set

VitaVitro by Shenzhen Vitavitro Bio-Tech Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction transfer catheter/set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 25bce283-0fc1-44c4-ba3d-38c8bef96d3f 33 fields · synced May 31, 2026