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Rapid Seal

FDA UDI

Class U (US FDA UDI)

by Aso LLC

Identity

Trade Name
Rapid Seal FDA UDI
Generic Name
Chitosan haemostatic agent, home-use FDA UDI
Device Name
Rapid Seal, Antibacterial Wound Gel, 28 uses, 2 tubes, 0.5 FL OZ each (14 ml) FDA UDI
Model / Reference
00017276237399 FDA UDI
Description
Rapid Seal, Antibacterial Wound Gel, 28 uses, 2 tubes, 0.5 FL OZ each (14 ml) FDA UDI

Identifiers

Catalog Number
B08JZLQF59 FDA UDI
Primary DI / UDI-DI
00017276237399 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Chitosan haemostatic agent, home-use FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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: Chitosan haemostatic agent, home-use

Rapid Seal by Aso LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chitosan haemostatic agent, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aso LLC

Sources (1)

  • FDA UDI 9d756336-2c83-4795-8adb-97719fa304f6 35 fields · synced Jun 8, 2026