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Transparent Dressing

FDA UDI

Class I (US FDA UDI)

by Aspen Surgical Products, Inc.

Identity

Trade Name
Transparent Dressing FDA UDI
Generic Name
Antimicrobial synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
The dressings are intended for wound care applications and securing objects to the skin. FDA UDI
Model / Reference
TD-27NS FDA UDI
Description
The dressings are intended for wound care applications and securing objects to the skin. FDA UDI

Identifiers

Primary DI / UDI-DI
00840113228447 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Antimicrobial synthetic polymer semi-permeable film dressing, adhesive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Antimicrobial synthetic polymer semi-permeable film dressing, adhesive

Transparent Dressing by Aspen Surgical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antimicrobial synthetic polymer semi-permeable film dressing, adhesive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6a37916e-0da0-4411-bd9b-3b7893a2535d 34 fields · synced Jun 9, 2026