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Extremity Care

FDA UDI

Class I (US FDA UDI)

by Extremity Care, Llc

Identity

Trade Name
Extremity Care FDA UDI
Generic Name
Syringe dispensing gun, single-use FDA UDI
Device Name
Control Dispenser FDA UDI
Model / Reference
ATL100S FDA UDI
Description
Control Dispenser FDA UDI

Identifiers

Primary DI / UDI-DI
00850003042305 FDA UDI
FDA Product Code
IQG FDA UDI
GMDN Term
Syringe dispensing gun, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Syringe dispensing gun, single-use

Extremity Care by Extremity Care, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Extremity Care, Llc

Sources (1)

  • FDA UDI 7ad33600-5739-484f-b268-c211f5ed1ea8 35 fields · synced May 30, 2026