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Invengenx

FDA UDI

Class II (US FDA UDI)

by Tisgenx

Identity

Trade Name
Invengenx FDA UDI
Generic Name
Cardiovascular patch, animal-derived FDA UDI
Model / Reference
XM-07 FDA UDI

Identifiers

Primary DI / UDI-DI
00850038226046 FDA UDI
510(k) Number
K182493 FDA UDI
FDA Product Code
FTM FDA UDI
GMDN Term
Cardiovascular patch, animal-derived FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 1 Centimeter FDA UDI
Length — 10 Centimeter FDA UDI

Category: Cardiovascular patch, animal-derived

Invengenx by Tisgenx — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiovascular patch, animal-derived.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tisgenx

Sources (1)

  • FDA UDI cb7cd5cd-e54f-4906-b60d-f2c66f390429 35 fields · synced May 30, 2026