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FillerCollector

FDA UDI

Class II (US FDA UDI)

by Human Med AG

Identity

Trade Name
FillerCollector FDA UDI
Generic Name
Surgical suction system collection container, reusable FDA UDI
Device Name
FillerCollector, Complete system for collection, filtration and concentration of fat tissue, Reusable FDA UDI
Model / Reference
Re-usable FillerCollector, Complete, Collect Fat FDA UDI
Description
FillerCollector, Complete system for collection, filtration and concentration of fat tissue, Reusable FDA UDI

Identifiers

Catalog Number
660000 FDA UDI
Primary DI / UDI-DI
04260170881366 FDA UDI
FDA Product Code
QKL FDA UDI
GMDN Term
Surgical suction system collection container, reusable 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

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical suction system collection container, reusable

FillerCollector by Human Med AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, reusable.

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 cf08cd37-0ae0-4c20-9daa-d18413213ecc 35 fields · synced May 30, 2026