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Transport Endoscopic Access Device

FDA UDI

Class II (US FDA UDI)

by USGI Medical

Identity

Trade Name
Transport Endoscopic Access Device FDA UDI
Generic Name
Multichannel gastrointestinal endoscopic guide, steerable FDA UDI
Device Name
Transport Endoscopic Access Device FDA UDI
Model / Reference
Transport-R FDA UDI
Description
Transport Endoscopic Access Device FDA UDI

Identifiers

Catalog Number
500100 FDA UDI
Primary DI / UDI-DI
00860009064751 FDA UDI
510(k) Number
K072405 FDA UDI
FDA Product Code
FED FDA UDI
ODB FDA UDI
GMDN Term
Multichannel gastrointestinal endoscopic guide, steerable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
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

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: Multichannel gastrointestinal endoscopic guide, steerable

Transport Endoscopic Access Device by USGI Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
USGI Medical

Sources (1)

  • FDA UDI 4fa9b8f7-797c-4fd4-95ef-092f4f290f2f 35 fields · synced May 30, 2026