← Back to catalogue

Stryker Fecal Management System

FDA UDI

Class I (US FDA UDI)

by Sage Products Llc

Identity

Trade Name
Stryker Fecal Management System FDA UDI
Generic Name
Faecal incontinence collector, skin-fixation FDA UDI
Device Name
Stryker Fecal Management System FDA UDI
Model / Reference
700-128 FDA UDI
Description
Stryker Fecal Management System FDA UDI

Identifiers

Catalog Number
700-128 FDA UDI
Primary DI / UDI-DI
00618029980274 FDA UDI
FDA Product Code
GDS FDA UDI
EXB FDA UDI
GMDN Term
Faecal incontinence collector, skin-fixation 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Faecal incontinence collector, skin-fixation

Stryker Fecal Management System by Sage Products Llc — Class I — 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
Sage Products Llc

Sources (1)

  • FDA UDI d6121f4f-ae93-425f-8f6f-b8bcfbb88d70 35 fields · synced Jun 8, 2026