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Bantex

FDA UDI

Class I (US FDA UDI)

by Solomed, S.A. de C.V.

Identity

Trade Name
Bantex FDA UDI
Generic Name
Pressure bandage, Hevea-latex, single-use, non-sterile FDA UDI
Device Name
Rubber Band Smarch FDA UDI
Model / Reference
6cm FDA UDI
Description
Rubber Band Smarch FDA UDI

Identifiers

Primary DI / UDI-DI
07500463968358 FDA UDI
FDA Product Code
MHW FDA UDI
GMDN Term
Pressure bandage, Hevea-latex, single-use, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

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

Yes

FDA UDI

Category: Pressure bandage, Hevea-latex, single-use, non-sterile

Bantex by Solomed, S.A. de C.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, Hevea-latex, single-use, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Solomed, S.A. de C.V.

Sources (1)

  • FDA UDI 6b950917-d337-4889-9364-f6327bac71c0 33 fields · synced May 31, 2026