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Activelife

FDA UDI

Class I (US FDA UDI)

by Convatec, Purchasing Department

Identity

Trade Name
ACTIVELIFE FDA UDI
Generic Name
One-piece intestinal ostomy bag, closed-ended FDA UDI
Device Name
ActiveLife One-Piece Pre-Cut Closed-End Pouch with Skin Barrier and Filter, with One Sided Comfort Panel, Transparent, 1 1/4 in (32 mm) FDA UDI
Model / Reference
175763 FDA UDI
Description
ActiveLife One-Piece Pre-Cut Closed-End Pouch with Skin Barrier and Filter, with One Sided Comfort Panel, Transparent, 1 1/4 in (32 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00768455102396 FDA UDI
FDA Product Code
EZQ FDA UDI
GMDN Term
One-piece intestinal ostomy bag, closed-ended FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5900 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Activelife by Convatec, Purchasing Department — Class I — 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

Sources (1)

  • FDA UDI 15390d8b-eee0-4550-b2aa-a9e72a3ff881 35 fields · synced May 31, 2026