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Calcium Alginate Dressing (6x6 in)

FDA UDI

Class I (US FDA UDI)

by Gentell

Identity

Trade Name
Calcium Alginate Dressing (6x6 in) FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial FDA UDI
Model / Reference
GEN-13700 FDA UDI

Identifiers

Catalog Number
GEN-13700 FDA UDI
Primary DI / UDI-DI
00361554000916 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Calcium Alginate Dressing (6x6 in) by Gentell — 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

Manufacturer
Gentell

Sources (1)

  • FDA UDI 0d4e632e-d250-4293-acfd-92606ed9cfe1 33 fields · synced May 30, 2026