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Kendall

FDA UDI

Class I (US FDA UDI)

by Extremity Care, Llc

Identity

Trade Name
Kendall FDA UDI
Generic Name
Dressing-fixation skin adhesive tape, non-silicone FDA UDI
Device Name
Kendall Waterproof Tape 1" x 10yd (2.5cm x 9.1m) FDA UDI
Model / Reference
EC007 FDA UDI
Description
Kendall Waterproof Tape 1" x 10yd (2.5cm x 9.1m) FDA UDI

Identifiers

Primary DI / UDI-DI
00850003042213 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Dressing-fixation skin adhesive tape, non-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

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

Dimensions & Sizes

Size
Width — 1 Inch FDA UDI
Length — 10 Yard FDA UDI

Category: Dressing-fixation skin adhesive tape, non-silicone

Kendall by Extremity Care, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Extremity Care, Llc

Sources (1)

  • FDA UDI dec79911-79dc-452b-b9ea-44cf133896f0 35 fields · synced May 30, 2026