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Kendall

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Kendall FDA UDI
Generic Name
Abdominal binder, single-use FDA UDI
Device Name
Kendall Buttonhole Belt with 2 Bobbins Pink and Blue 2-3/8" x 48" (6 cm x 1.2 m) FDA UDI
Model / Reference
31410270B FDA UDI
Description
Kendall Buttonhole Belt with 2 Bobbins Pink and Blue 2-3/8" x 48" (6 cm x 1.2 m) FDA UDI

Identifiers

Catalog Number
31410270B- FDA UDI
Primary DI / UDI-DI
20192253021049 FDA UDI
FDA Product Code
FSD FDA UDI
GMDN Term
Abdominal binder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5160 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 48 Inch FDA UDI
Width — 2.38 Inch FDA UDI

Category: Abdominal binder, single-use

Kendall by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal binder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4abd616d-7f71-4288-80a4-1b96cb05f4eb 35 fields · synced Jun 8, 2026