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First Aid Only

FDA UDI

Class I (US FDA UDI)

by Acme United Corp.

Identity

Trade Name
First Aid Only FDA UDI
Generic Name
Snake/insect venom suction device FDA UDI
Device Name
Snake bite kit FDA UDI
Model / Reference
7103 FDA UDI
Description
Snake bite kit FDA UDI

Identifiers

Catalog Number
7103 FDA UDI
Primary DI / UDI-DI
00738743071031 FDA UDI
FDA Product Code
KYP FDA UDI
GMDN Term
Snake/insect venom suction device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5740 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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: Snake/insect venom suction device

First Aid Only by Acme United Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Snake/insect venom suction device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Acme United Corp.

Sources (1)

  • FDA UDI 9f1748a2-ff95-4c92-891a-df97d2fd292b 35 fields · synced Jun 20, 2026