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traxi Panniculus Retractor Extender

EUDAMEDFDA UDI

Class I (EU MDR)

Ref PRS-0550Model PRS-0530

by Clinical Innovations, LLC

Identity

Trade Name
traxi Panniculus Retractor Extender EUDAMED
traxi® Panniculus Retractor Extender FDA UDI
Generic Name
Abdominal retractor, hand-held FDA UDI
Device Name
traxi Panniculus Retractor EUDAMED
Traxi Extender with Retentus Technology (BMI>50 - used with PH-25) FDA UDI
Model / Reference
PRS-0530 EUDAMED
PRS-0550 EUDAMEDFDA UDI
Description
Traxi Extender with Retentus Technology (BMI>50 - used with PH-25) FDA UDI

Identifiers

Primary DI / UDI-DI
30814247020360 EUDAMEDFDA UDI
Basic UDI-DI
0814247001030QV EUDAMED
Unit of Use DI
00814247020369 EUDAMED
FDA Product Code
CCX FDA UDI
EMDN Code
Z12080399 VARIOUS CHILDBIRTH SUPPORT AND MATERNAL ASSISTANCE INSTRUMENTS - OTHER EUDAMED
GMDN Term
Abdominal retractor, hand-held FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.6820 FDA UDI
Market of Registration
Italy 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

Yes

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

Yes

FDA UDI

traxi Panniculus Retractor Extender by Clinical Innovations, LLC — Class I — 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-000031386
Authorised Representative
MVF FR-AR-000011189

Sources (2)

  • EUDAMED e293a04f-c049-4afd-b27b-6c1f13c608c3 61 fields · synced Jul 13, 2026
  • FDA UDI 55bbfc5b-dd10-414f-a0c3-abae8b94ed40 33 fields · synced May 30, 2026