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Riptide™ Aspiration Pump MAP-1000

by Micro Therapeutics, Inc.

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 Number00763000950750 UDI-DI Date9 Mar 2026ListedStatusListed 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  • Withdrawn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
Riptide™ Aspiration Pump
Generic Name
Surgical irrigation/aspiration pump, reusable
Model / Reference
MAP-1000
Primary DI / UDI-DI
00763000950750
510(k) Number
FDA Product Code
NRY
GMDN Term
Surgical irrigation/aspiration pump, reusable
Device Class
Class II
Regulation Number
870.1250
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Cleared under the same submission (K243080)

Other devices from Micro Therapeutics, Inc.

See all devices from Micro Therapeutics, Inc. →

Properties

  • Contains Latex
  • Prescription Use
  • Serial Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No