← Back to catalogue

Infinity

FDA UDI

Class II (US FDA UDI)

by US Endoscopy

Identity

Trade Name
Infinity FDA UDI
Generic Name
Flexible endoscopic cytology brush, single-use FDA UDI
Device Name
The disposable Infinity ERCP sampling device is used to retrieve cytological cell samples in the gastrointestinal tract. FDA UDI
Model / Reference
00711653 FDA UDI
Description
The disposable Infinity ERCP sampling device is used to retrieve cytological cell samples in the gastrointestinal tract. FDA UDI

Identifiers

Catalog Number
00711653 FDA UDI
Primary DI / UDI-DI
00816765012758 FDA UDI
FDA Product Code
FDX FDA UDI
GMDN Term
Flexible endoscopic cytology brush, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3 Millimeter FDA UDI

Infinity by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
US Endoscopy

Sources (1)

  • FDA UDI 9188ed9c-fb93-4f1e-a0c6-e4c1c7d2254e 38 fields · synced May 31, 2026