← Back to catalogue

New Image

FDA UDI

Class I (US FDA UDI)

by Hollister Incorporated

Identity

Trade Name
New Image FDA UDI
Generic Name
Multiple-piece urostomy bag, open-ended FDA UDI
Device Name
2-Piece Urostomy Pouch FDA UDI
Model / Reference
18924 FDA UDI
Description
2-Piece Urostomy Pouch FDA UDI

Identifiers

Catalog Number
18924 FDA UDI
Primary DI / UDI-DI
00610075187973 FDA UDI
FDA Product Code
EXG FDA UDI
GMDN Term
Multiple-piece urostomy bag, open-ended FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

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

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 70 Millimeter FDA UDI

Category: Multiple-piece urostomy bag, open-ended

New Image by Hollister Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-piece urostomy bag, open-ended.

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

Sources (1)

  • FDA UDI 1e7e408e-3982-4a41-bdd9-f5ce877984a4 36 fields · synced Jun 9, 2026