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AngioSystems Pressure Dressing

FDA UDI

Class U (US FDA UDI)

by Angiosystems, Incorporated

Identity

Trade Name
AngioSystems Pressure Dressing FDA UDI
Generic Name
Cavity-wound management dressing, non-antimicrobial FDA UDI
Model / Reference
8000 FDA UDI

Identifiers

Primary DI / UDI-DI
00816611024898 FDA UDI
510(k) Number
K864688 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Cavity-wound management dressing, non-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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cavity-wound management dressing, non-antimicrobial

AngioSystems Pressure Dressing by Angiosystems, Incorporated — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cavity-wound management dressing, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Angiosystems, Incorporated

Sources (1)

  • FDA UDI 2b490f52-2a86-4e86-a26d-e7bd70474f44 33 fields · synced Jun 1, 2026