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Evulse

FDA UDI

Class I (US FDA UDI)

by Innovative Med, Inc.

Identity

Trade Name
Evulse FDA UDI
Generic Name
Autologous adipose tissue noninvasive processing set FDA UDI
Device Name
LTM EVULSE, DOUBL, 500 & 1500 FDA UDI
Model / Reference
LTM-Evu D 5-15 FDA UDI
Description
LTM EVULSE, DOUBL, 500 & 1500 FDA UDI

Identifiers

Primary DI / UDI-DI
00851314007489 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Autologous adipose tissue noninvasive processing set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Autologous adipose tissue noninvasive processing set

Evulse by Innovative Med, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autologous adipose tissue noninvasive processing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0a65d3eb-cb1e-4243-98e7-4b07724825f1 34 fields · synced Jun 8, 2026