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TRULINK NIBP Hoses and adapters

by Spacelabs Healthcare (Washington), Inc 29 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10841522101120 UDI-DI Date14 Mar 2017ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Trulink
Generic Name
Blood pressure cuff, reusable
Model / Ref / Catalog
NIBP Hoses and adapters, 712-0152-01
Primary DI / UDI-DI
10841522101120
510(k) Number
FDA Product Code
DXQ
GMDN Term
Blood pressure cuff, reusable
Device Class
Class II
Regulation Number
870.1120
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood pressure cuff, reusable

Cleared under the same submission (K954282)

Show all (12)

Other devices from Spacelabs Healthcare (Washington), Inc

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Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No