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Optiheal Silicone Postsurgical Dressing

FDA UDI

Class I (US FDA UDI)

by Neo G USA Inc

Identity

Trade Name
Optiheal Silicone Postsurgical Dressing FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
Silicone Postsurgical Dressing 8x4in / 20x10cm FDA UDI
Model / Reference
AW002A FDA UDI
Description
Silicone Postsurgical Dressing 8x4in / 20x10cm FDA UDI

Identifiers

Catalog Number
AW002 FDA UDI
Primary DI / UDI-DI
00819333029028 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound-nonadherent dressing, absorbent, non-antimicrobial

Optiheal Silicone Postsurgical Dressing by Neo G USA Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, absorbent, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neo G USA Inc

Sources (1)

  • FDA UDI 9483960c-80cc-49f6-bd85-2dea5d9d5d78 34 fields · synced Jun 1, 2026