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Bedal

FDA UDI

Class I (US FDA UDI)

by Bedal

Identity

Trade Name
Bedal FDA UDI
Generic Name
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
Sterilized FDA UDI
Model / Reference
bedal air S FDA UDI
Description
Sterilized FDA UDI

Identifiers

Catalog Number
UN02 FDA UDI
Primary DI / UDI-DI
05430000258401 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 78 Millimeter FDA UDI
Width — 38.8 Millimeter FDA UDI
Height — 11.1 Millimeter FDA UDI

Category: Synthetic polymer semi-permeable film dressing, adhesive

Bedal by Bedal — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic polymer semi-permeable film dressing, adhesive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bedal

Sources (1)

  • FDA UDI 662b141b-8839-403c-ae78-9cf153f53267 37 fields · synced Jun 8, 2026