← Back to catalogue

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
Non Sterilized FDA UDI
Model / Reference
bedal picc/cvc FDA UDI
Description
Non Sterilized FDA UDI

Identifiers

Catalog Number
PCNS02 FDA UDI
Primary DI / UDI-DI
05430000258524 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

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

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 78 Millimeter FDA UDI
Width — 38.8 Millimeter FDA UDI
Height — 10.2 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Bedal

Sources (1)

  • FDA UDI 7a6b5bf4-8f9d-4baf-9d58-96ee4c5ca52c 37 fields · synced May 30, 2026