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BlastX

FDA UDI

Class U (US FDA UDI)

by Next Science LLC

Identity

Trade Name
BlastX FDA UDI
Generic Name
Wound hydrogel dressing, antimicrobial FDA UDI
Model / Reference
WG-0003 FDA UDI

Identifiers

Primary DI / UDI-DI
00370858000355 FDA UDI
510(k) Number
K163188 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound hydrogel dressing, antimicrobial 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound hydrogel dressing, antimicrobial

BlastX by Next Science LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Next Science LLC

Sources (1)

  • FDA UDI ed26bd67-4c10-4a8f-a9b0-f7afcb8ded88 33 fields · synced Jun 8, 2026