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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, single-use FDA UDI
Device Name
Single-use FillerCollector - complete system for collection, filtration and concentration of fat tissue, 250ml FDA UDI
Model / Reference
Single-use FillerCollector, 250ml, Collect Fat FDA UDI
Description
Single-use FillerCollector - complete system for collection, filtration and concentration of fat tissue, 250ml FDA UDI

Identifiers

Catalog Number
1660000-5 FDA UDI
Primary DI / UDI-DI
04260170881083 FDA UDI
FDA Product Code
QKL FDA UDI
GMDN Term
Surgical suction system collection container, single-use 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical suction system collection container, single-use

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, single-use.

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 9c11f6f6-e172-47d7-afdb-44ae0b975565 36 fields · synced Jun 1, 2026