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Medline DYNJAAC400PM

by Medline Industries, Inc.

Medline DYNJAAC400PM is a Class II device made by Medline Industries, Inc., cleared under FDA 510(k) K111282 on 11 Aug 2011 and listed in FDA GUDID since 14 Oct 2016 (UDI-DI 10080196551668), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K111282

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10080196551668 UDI-DI Date14 Oct 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK111282 Date11 Aug 2011DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K111282 decided 11 Aug 2011 Active
  • FDA GUDID UDI-DI 10080196551668 listed 14 Oct 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K111282
  2. Listed FDA GUDID 10080196551668

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Medline
Generic name
Electrical-only medical device connection cable, reusable
Model / Ref / Catalog
DYNJAAC400PM
Primary DI / UDI-DI
10080196551668
510(k) Number
FDA product code
FLL
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)