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Purilon

FDA UDI

Class I (US FDA UDI)

by Coloplast A/S

Identity

Trade Name
Purilon FDA UDI
Generic Name
Wound hydrogel dressing, non-antimicrobial FDA UDI
Model / Reference
3900 FDA UDI

Identifiers

Catalog Number
3900 FDA UDI
Primary DI / UDI-DI
05708932759557 FDA UDI
FDA Product Code
NAE FDA UDI
GMDN Term
Wound hydrogel dressing, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4022 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Weight — 15 Gram FDA UDI

Category: Wound hydrogel dressing, non-antimicrobial

Purilon by Coloplast A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Coloplast A/S

Sources (1)

  • FDA UDI 03026c5a-9db5-4b49-b599-f363c794dc63 36 fields · synced Jun 1, 2026