← Back to catalogue
GEMS Soft Harvest System
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref DC1SLTON1320-01Model DC1SLCAR1315-01
Identity
- Trade Name
- GEMS Soft Harvest System EUDAMEDTulip GEMS™ Single-Use FDA UDI
- Generic Name
- Liposuction system cannula, single-use FDA UDI
- Device Name
- GEMS Carraway Harvester EUDAMEDGEMS - Premium Single-Use Tonnard SuperLuerLok 2.41mm OD(1.96mm ID) x 20cm - Single FDA UDI
- Model / Reference
- DC1SLCAR1315-01 EUDAMEDDC1SLTON1320-01 EUDAMEDFDA UDI
- Description
- GEMS - Premium Single-Use Tonnard SuperLuerLok 2.41mm OD(1.96mm ID) x 20cm - Single FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00819127021627 EUDAMEDFDA UDI
- Basic UDI-DI
- 081912702DCHVST59 EUDAMED
- Direct Marketing DI
- 00819127021627 EUDAMED
- FDA Product Code
- QPB FDA UDI
- EMDN Code
- K01020110 MINIMALLY INVASIVE SURGERY CANNULAS, SINGLE-USE EUDAMED
- GMDN Term
- Liposuction system cannula, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 081912702DCHVST59 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Tulip Medical Products, Inc.
- EUDAMED SRN
- US-MF-000049097
- Authorised Representative
- MedEnvoy Global BV NL-AR-000024028
Sources (2)
- EUDAMED fca31d88-6a30-4d47-aa1a-d039a8e2bb42 61 fields · synced Jun 20, 2026
- FDA UDI 01218d6c-f6a9-4649-badb-a3e700c16ba3 33 fields · synced May 29, 2026