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Q-graft centrifugation set

FDA UDI

Class I (US FDA UDI)

by Human Med AG

Identity

Trade Name
Q-graft centrifugation set FDA UDI
Generic Name
Stromal vascular fraction recovery set FDA UDI
Device Name
Q-graft centrifugation set, for the intraoperative separation of regenerative cells (stromal vascular fraction/ SVF) from adipose tissue FDA UDI
Model / Reference
Single-use Centrifugation Set for Q-graft FDA UDI
Description
Q-graft centrifugation set, for the intraoperative separation of regenerative cells (stromal vascular fraction/ SVF) from adipose tissue FDA UDI

Identifiers

Catalog Number
300003 FDA UDI
Primary DI / UDI-DI
04260170881618 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Stromal vascular fraction recovery set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Stromal vascular fraction recovery set

Q-graft centrifugation set by Human Med AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stromal vascular fraction recovery set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Human Med AG

Sources (1)

  • FDA UDI 358e37fd-8fdc-4000-b248-89441c110538 35 fields · synced May 30, 2026