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Avacen

FDA UDI

Class II (US FDA UDI)

by Avacen Medical, Inc

Identity

Trade Name
AVACEN FDA UDI
Generic Name
Electric pad localized-body heating system FDA UDI
Device Name
Vacuum Chamber Insert (VCI) FDA UDI
Model / Reference
VCI FDA UDI
Description
Vacuum Chamber Insert (VCI) FDA UDI

Identifiers

Primary DI / UDI-DI
00862800000310 FDA UDI
510(k) Number
K133981 FDA UDI
FDA Product Code
IRT FDA UDI
GMDN Term
Electric pad localized-body heating system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electric pad localized-body heating system

Avacen by Avacen Medical, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric pad localized-body heating system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avacen Medical, Inc

Sources (1)

  • FDA UDI f6514a67-65d9-4c20-8ede-36620abedd75 36 fields · synced May 29, 2026