← Back to catalogue

FifthPulse

FDA UDI

Class I (US FDA UDI)

by Jeg & Sons Inc.

Identity

Trade Name
FifthPulse FDA UDI
Generic Name
Dressing-fixation skin adhesive tape, silicone FDA UDI
Device Name
Medical Silicone Gel Tape FDA UDI
Model / Reference
1 roll FDA UDI
Description
Medical Silicone Gel Tape FDA UDI

Identifiers

Catalog Number
FMN100523 FDA UDI
Primary DI / UDI-DI
00810084936863 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dressing-fixation skin adhesive tape, silicone

FifthPulse by Jeg & Sons Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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
Jeg & Sons Inc.

Sources (1)

  • FDA UDI 9623d6eb-a027-44c8-8e85-34231e76a613 34 fields · synced May 30, 2026