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Axiom® SeroVac® 225

by Axiom Medical, Incorporated

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 NumberM6652250 UDI-DI Date23 Sep 2018ListedStatusListed 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  • Withdrawn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
Axiom® SeroVac®
Generic Name
Closed-wound drain, non-bioabsorbable
Model / Reference
225
Primary DI / UDI-DI
M6652250
510(k) Number
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
Size
Length — 5.2 Inch
Total Volume — 10 Milliliter

Related devices

Category: Closed-wound drain, non-bioabsorbable

Cleared under the same submission (K965146)

Show all (12)

Other devices from Axiom Medical, Incorporated

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Properties

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

Other properties (8)

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