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KerraCel Ag

FDA UDI

Class U (US FDA UDI)

by Crawford Healthcare Limited

Identity

Trade Name
KerraCel Ag FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial FDA UDI
Model / Reference
0.75 x 18in FDA UDI

Identifiers

Catalog Number
CWL1162 FDA UDI
Primary DI / UDI-DI
05060077233652 FDA UDI
510(k) Number
K162508 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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 — 18 Inch FDA UDI
Height — 0.75 Inch FDA UDI

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

KerraCel Ag by Crawford Healthcare Limited — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 284058aa-98fa-4f97-b34d-90d6f5c07d31 37 fields · synced Jun 8, 2026