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Extraction tube

FDA UDI

Class II (US FDA UDI)

by Human Med AG

Identity

Trade Name
Extraction tube FDA UDI
Generic Name
Collection syringe adaptor, single-use FDA UDI
Device Name
Single-use Extraction Tube for all HM Collectors, For extracting the fat from the container into syringes FDA UDI
Model / Reference
Single-use Extraction Tube for all HM Collectors, Collect Fat FDA UDI
Description
Single-use Extraction Tube for all HM Collectors, For extracting the fat from the container into syringes FDA UDI

Identifiers

Catalog Number
671510-5 FDA UDI
Primary DI / UDI-DI
04260170881502 FDA UDI
FDA Product Code
QKL FDA UDI
GMDN Term
Collection syringe adaptor, 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: Collection syringe adaptor, single-use

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

Similar devices

Also classified as Collection syringe adaptor, 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 3d3cfeea-896e-4d88-aeb1-d6b6d13bee12 35 fields · synced May 30, 2026