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Transport Retroflex

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 118180

by USGI Medical

Identity

Trade Name
Transport Retroflex EUDAMED
Transport Endoscopic Access Device FDA UDI
Generic Name
Multichannel gastrointestinal endoscopic guide, steerable FDA UDI
Device Name
Transport Retroflex EUDAMED
Transport Endoscopic Access Device FDA UDI
Model / Reference
118180 EUDAMED
Transport Retroflex FDA UDI
Description
Transport Endoscopic Access Device FDA UDI

Identifiers

Catalog Number
118180 FDA UDI
Primary DI / UDI-DI
00860009064706 EUDAMEDFDA UDI
Basic UDI-DI
B-00860009064706 EUDAMED
510(k) Number
K072405 FDA UDI
FDA Product Code
ODB FDA UDI
FED FDA UDI
EMDN Code
G030899 INSTRUMENTS FOR GASTRO-INTESTINAL ENDOSCOPY AND ECO-ENDOSCOPY, SINGLE-USE - OTHER EUDAMED
GMDN Term
Multichannel gastrointestinal endoscopic guide, steerable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Market of Registration
Spain 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue morcellation system handpiece, line-powered

Transport Retroflex by USGI Medical — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue morcellation system handpiece, line-powered.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
USGI Medical
EUDAMED SRN
US-MF-000031970
Authorised Representative
MPS Medical Product Service GmbH DE-AR-000005009

Sources (2)

  • EUDAMED 5d0e47cd-d934-4f08-940c-f178abb11b06 61 fields · synced Jun 18, 2026
  • FDA UDI 0ab4728a-5a30-4fee-882b-49cbac541603 35 fields · synced May 30, 2026