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Bell-Horn

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
BELL-HORN FDA UDI
Generic Name
Compression/pressure sock/stocking, single-use FDA UDI
Device Name
WHISPER 20-30MMHG KN CT TR BG, XXXXL FDA UDI
Model / Reference
200004X FDA UDI
Description
WHISPER 20-30MMHG KN CT TR BG, XXXXL FDA UDI

Identifiers

Primary DI / UDI-DI
00888912266499 FDA UDI
FDA Product Code
DWL FDA UDI
GMDN Term
Compression/pressure sock/stocking, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Compression/pressure sock/stocking, single-use

Unlock the full potential of your patients' health with BELL-HORN, a cutting-edge compression/pressure sock/stocking designed to provide targeted support for circulation and vein health. This single-use device features advanced elastic material for secure fit and comfort, while also incorporating antimicrobial properties to prevent infection.

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 0c5ae6d8-8fbe-4784-8a57-375461027de1 33 fields · synced Jul 20, 2026