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SyntrFuge System 30

FDA UDI

Class II (US FDA UDI)

by Syntr Health Technologies, Inc.

Identity

Trade Name
SyntrFuge System 30 FDA UDI
Generic Name
Autologous adipose tissue noninvasive processing set FDA UDI
Device Name
Fat microsizing Unit. FDA UDI
Model / Reference
90-1003 FDA UDI
Description
Fat microsizing Unit. FDA UDI

Identifiers

Catalog Number
90-1003 FDA UDI
Primary DI / UDI-DI
00860005496723 FDA UDI
FDA Product Code
QKL FDA UDI
GMDN Term
Autologous adipose tissue noninvasive processing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 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: Autologous adipose tissue noninvasive processing set

SyntrFuge System 30 by Syntr Health Technologies, Inc. — Class II — 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 c21edf54-ae2e-427c-ad6d-2434dbde42b0 35 fields · synced Jun 8, 2026