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Tulip GEMS™ Single-Use

FDA UDI

by Tulip Medical Products, Inc.

Identity

Trade Name
Tulip GEMS™ Single-Use FDA UDI
Generic Name
Autologous adipose tissue reinjection set FDA UDI
Device Name
Tulip Single Use, One Patient Gold Kit Plus Injectors FDA UDI
Model / Reference
DPK-GOLD+INJ-01 FDA UDI
Description
Tulip Single Use, One Patient Gold Kit Plus Injectors FDA UDI

Identifiers

Primary DI / UDI-DI
00819127024093 FDA UDI
GMDN Term
Autologous adipose tissue reinjection set FDA UDI

Classification

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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Autologous adipose tissue reinjection set

Tulip GEMS™ Single-Use by Tulip Medical Products, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autologous adipose tissue reinjection set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1c24b997-538e-477d-a136-640196dfee0e 33 fields · synced Jun 9, 2026