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AtriAmp

FDA UDI

Class II (US FDA UDI)

by Atrility Medical, LLC

Identity

Trade Name
AtriAmp FDA UDI
Generic Name
Electrical-only medical device connection cable, single-use FDA UDI
Device Name
AtriAmp FDA UDI
Model / Reference
10001 FDA UDI
Description
AtriAmp FDA UDI

Identifiers

Primary DI / UDI-DI
00860004773702 FDA UDI
510(k) Number
K200674 FDA UDI
FDA Product Code
DSA FDA UDI
IKD FDA UDI
GMDN Term
Electrical-only medical device connection cable, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 FDA UDI
890.1175 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

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
Radiation Sterilization FDA UDI

Category: Electrical-only medical device connection cable, single-use

AtriAmp by Atrility Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, single-use.

Cleared under the same submission

K200674 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atrility Medical, LLC

Sources (1)

  • FDA UDI 417c3b9c-a845-40f2-b347-825b9f8a1cb2 34 fields · synced Jun 8, 2026