Identity

Trade Name
FIRSTAR FDA UDI
Generic Name
First aid kit, non-medicated, single-use FDA UDI
Device Name
First aid and dressing FDA UDI
Model / Reference
91018S74 FDA UDI
Description
First aid and dressing FDA UDI

Identifiers

Primary DI / UDI-DI
B44891018S741 FDA UDI
GMDN Term
First aid kit, non-medicated, single-use FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Safe FDA UDI

Category: First aid kit, non-medicated, single-use

Firstar by Firstar Healthcare Company Limited (guangzhou) — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 93e7498f-5050-454d-8d38-efd1993dd19e 33 fields · synced Jun 8, 2026