← Back to catalogue

GEMS Soft Harvest System

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref DATLLLL2.4mm-01Model Disposable NanoFat Transfer, Generation 1- Cartridge (Single)

by Tulip Medical Products, Inc.

Identity

Trade Name
GEMS Soft Harvest System EUDAMED
Tulip GEMS™ Single-Use FDA UDI
Generic Name
Autologous adipose tissue reinjection set FDA UDI
Device Name
DNTC-01 EUDAMED
Single-Use Transparent 2.4mm Transfer - Female to Female Luer Lock - Sterile Pack of 1 FDA UDI
Model / Reference
Disposable NanoFat Transfer, Generation 1- Cartridge (Single) EUDAMED
DATLLLL2.4mm-01 EUDAMEDFDA UDI
Description
Single-Use Transparent 2.4mm Transfer - Female to Female Luer Lock - Sterile Pack of 1 FDA UDI

Identifiers

Primary DI / UDI-DI
00819127022266 EUDAMEDFDA UDI
Basic UDI-DI
081912702TRANSFERZL EUDAMED
Direct Marketing DI
00819127022266 EUDAMED
FDA Product Code
QPB FDA UDI
EMDN Code
Z12040214 LIPOSUCTION SYSTEMS EUDAMED
GMDN Term
Autologous adipose tissue reinjection set FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
878.5040 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

GEMS Soft Harvest System by Tulip Medical Products, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000049097
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (2)

  • EUDAMED 92446d76-b4ed-4968-a6ac-483e27550e61 61 fields · synced Jun 19, 2026
  • FDA UDI de64770b-4415-44b0-b12a-e21dc3f20748 33 fields · synced May 30, 2026