Fever Scout Adhesive Refill

FDA UDI

Class I (US FDA UDI)

by VivaLNK, Inc.

Identity

Trade Name: Fever Scout Adhesive Refill FDA UDI
Generic Name: Dressing-fixation skin adhesive tape, silicone FDA UDI
Device Name: The silicon patch is a small, thin layer of soft silicon used for the adherence of specific sensor. FDA UDI
Model / Reference: VV200A FDA UDI
Description: The silicon patch is a small, thin layer of soft silicon used for the adherence of specific sensor. FDA UDI

Identifiers

Primary DI / UDI-DI: 00865064000133 FDA UDI
FDA Product Code: KGX FDA UDI
GMDN Term: Dressing-fixation skin adhesive tape, silicone FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5240 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Dressing-fixation skin adhesive tape, silicone

Fever Scout Adhesive Refill by VivaLNK, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing-fixation skin adhesive tape, silicone.

ComfiTape — DERMARITE INDUSTRIES LLC · Class I
Acanthus — ACANTHUS MEDICAL CREATIONS, LLC · Class I
Silicone Bandage — AP MDS Co., Ltd. · Class I
McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class I
FifthPulse — Jeg & Sons Inc. · Class I
OFFSET MODULAR HEAD PROVISIONAL — Biomet Orthopedics, Inc. · Class I
Acanthus — ACANTHUS MEDICAL CREATIONS, LLC · Class I
LotFancy — Henan Maidingkang Medical Technology Co., Ltd. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: VivaLNK, Inc.

Sources (1)

FDA UDI c9f82c41-e72f-4ebe-8778-258db09126ad 34 fields · synced Jun 8, 2026