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Omniplug Collagen Wound Dressing

FDA UDI

Class U (US FDA UDI)

by Maxigen Biotech Inc.

Identity

Trade Name
Omniplug Collagen Wound Dressing FDA UDI
Generic Name
General oral wound dressing, animal-derived FDA UDI
Model / Reference
HAD001020 FDA UDI

Identifiers

Primary DI / UDI-DI
04714691213132 FDA UDI
510(k) Number
K230529 FDA UDI
FDA Product Code
OLR FDA UDI
GMDN Term
General oral wound dressing, animal-derived 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: General oral wound dressing, animal-derived

Omniplug Collagen Wound Dressing by Maxigen Biotech Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General oral wound dressing, animal-derived.

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 7bde721b-b6ee-4c64-b4b9-20f2fa1fa7e9 33 fields · synced May 30, 2026