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Sequa® Cel

FDA UDI

Class I (US FDA UDI)

by Foshan United Medical Technologies Ltd.

Identity

Trade Name
Sequa® Cel FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial FDA UDI
Device Name
Sequa®Cel CMC Dressing is a sterile nonwoven wound dressing composed of 100% Carboxymethyl Cellulose (CMC) fibers. The Sequa®Cel CMC Dressing is highly absorbent, conformable and wet integral. As wound exudates are absorbed, the CMC fibers form a soft gel which assists to keep a moist environment to support the wound healing process and promote the removal of nonviable tissue from the wound, without damaging newly formed tissue FDA UDI
Model / Reference
5x5cm FDA UDI
Description
Sequa®Cel CMC Dressing is a sterile nonwoven wound dressing composed of 100% Carboxymethyl Cellulose (CMC) fibers. The Sequa®Cel CMC Dressing is highly absorbent, conformable and wet integral. As wound exudates are absorbed, the CMC fibers form a soft gel which assists to keep a moist environment to support the wound healing process and promote the removal of nonviable tissue from the wound, without damaging newly formed tissue FDA UDI

Identifiers

Catalog Number
SQC0505 FDA UDI
Primary DI / UDI-DI
06931132201017 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

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: Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial

Sequa® Cel by Foshan United Medical Technologies Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b1f11806-4315-4655-b537-8b7f1e9d5079 34 fields · synced May 30, 2026