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ReSolve®, MAK-NV™ 00884450014059

by Merit Medical Systems, Inc.

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

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 Number00884450014059 UDI-DI Date16 Feb 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
ReSolve®, MAK-NV™
Generic Name
Closed-wound drain, non-bioabsorbable
Model / Ref / Catalog
00884450014059, RLC-NV-12
Primary DI / UDI-DI
00884450014059
FDA Product Code
GBX
GMDN Term
Closed-wound drain, non-bioabsorbable
Device Class
Class I
Regulation Number
878.4200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Closed-wound drain, non-bioabsorbable

Other devices from Merit Medical Systems, Inc.

See all devices from Merit Medical Systems, Inc. →

Properties

  • Sterile
  • Single Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No