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WellCare

FDA UDI

Class I (US FDA UDI)

by Wellcare International, Inc.

Identity

Trade Name
WellCare FDA UDI
Generic Name
Thermal vapour lung treatment system catheter FDA UDI
Device Name
WellCare 7 mil exam Blue nitrile gloves, size L, 100pcs/box, 10boxes/case FDA UDI
Model / Reference
WNB703 FDA UDI
Description
WellCare 7 mil exam Blue nitrile gloves, size L, 100pcs/box, 10boxes/case FDA UDI

Identifiers

Primary DI / UDI-DI
00682670682597 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Thermal vapour lung treatment system catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Thermal vapour lung treatment system catheter

WellCare by Wellcare International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thermal vapour lung treatment system catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eab9b864-bf6d-47fd-852c-1484bb065332 33 fields · synced Jun 1, 2026