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DropSafe™ Inject-Safe Barrier Bandage™

FDA UDI

Class I (US FDA UDI)

by Htl Strefa S A

Identity

Trade Name
DropSafe™ Inject-Safe Barrier Bandage™ FDA UDI
Generic Name
Skin adhesive protective material FDA UDI
Device Name
Barrier Bandage it’s intended to contain post-injection bleeding during a subcutaneous or intramuscular injection. The device is intended for healthcare professions (HCP) and lay users. The device is an OTC product. FDA UDI
Model / Reference
n/a FDA UDI
Description
Barrier Bandage it’s intended to contain post-injection bleeding during a subcutaneous or intramuscular injection. The device is intended for healthcare professions (HCP) and lay users. The device is an OTC product. FDA UDI

Identifiers

Catalog Number
6070 FDA UDI
Primary DI / UDI-DI
05907996099979 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Skin adhesive protective material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin adhesive protective material

DropSafe™ Inject-Safe Barrier Bandage™ by Htl Strefa S A — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin adhesive protective material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Htl Strefa S A

Sources (1)

  • FDA UDI f25435b0-0849-490a-8ac8-9dd463d4b0b5 34 fields · synced May 30, 2026