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Adaptic®

FDA UDI

Class I (US FDA UDI)

by Systagenix Wound Management, Limited

Identity

Trade Name
ADAPTIC® FDA UDI
Generic Name
Wound-nonadherent dressing, permeable, non-antimicrobial FDA UDI
Device Name
Non-Adhering Dressing FDA UDI
Model / Reference
2014 FDA UDI
Description
Non-Adhering Dressing FDA UDI

Identifiers

Catalog Number
2014 FDA UDI
Primary DI / UDI-DI
15051978000167 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Wound-nonadherent dressing, permeable, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 40.6 Centimeter FDA UDI
Width — 7.6 Centimeter FDA UDI

Category: Wound-nonadherent dressing, permeable, non-antimicrobial

Adaptic® by Systagenix Wound Management, Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, permeable, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Systagenix Wound Management, Limited

Sources (1)

  • FDA UDI e7799a4a-e3c6-467f-a05f-05c8efd52b06 36 fields · synced May 30, 2026