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Sensoronics SC-MANE-8AMP

by Sensoronics Incorporated

Sensoronics SC-MANE-8AMP is a Class II device made by Sensoronics Incorporated, listed in FDA GUDID since 12 Oct 2016 (UDI-DI 00851457007032), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851457007032 UDI-DI Date12 Oct 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sensoronics
Generic name
Electrical-only medical device connection cable, reusable
Model / reference
SC-MANE-8AMP
Primary DI / UDI-DI
00851457007032
FDA product code
DSA
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class II
Regulation number
870.2900
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrical-only medical device connection cable, reusable

Similar devices in this category

Other devices filed under Electrical-only medical device connection cable, reusable.

Other devices from Sensoronics Incorporated

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Properties

  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (12, all answered No)