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ViveCare

FDA UDI

Class I (US FDA UDI)

by Vive Health Llc

Identity

Trade Name
ViveCare FDA UDI
Generic Name
Multiple-piece intestinal ostomy bag, closed-ended FDA UDI
Device Name
Ostomy Bags Two-Piece (Hook and Loop) 21PK FDA UDI
Model / Reference
LVA3052HLO21CT FDA UDI
Description
Ostomy Bags Two-Piece (Hook and Loop) 21PK FDA UDI

Identifiers

Primary DI / UDI-DI
00810113577104 FDA UDI
FDA Product Code
FON FDA UDI
GMDN Term
Multiple-piece intestinal ostomy bag, closed-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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple-piece intestinal ostomy bag, closed-ended

ViveCare by Vive Health Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple-piece intestinal ostomy bag, closed-ended.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vive Health Llc

Sources (1)

  • FDA UDI 83df1f1e-baba-4caf-820c-db76dfa94483 33 fields · synced Jun 8, 2026