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LifeGlobal™ CodaAir™ Positive Pressure Unit, 230V

by CooperSurgical, 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 Number00888937034264 UDI-DI Date4 Aug 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  • Withdrawn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
LifeGlobal™
Generic Name
Non-respiratory device ambient air filter
Model / Ref / Catalog
CodaAir™ Positive Pressure Unit, 230V, CAPP-230-M
Primary DI / UDI-DI
00888937034264
510(k) Number
FDA Product Code
MQG
GMDN Term
Non-respiratory device ambient air filter
Device Class
Class II
Regulation Number
884.6120
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K001486)

Show all (12)

Other devices from CooperSurgical, Inc.

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Properties

  • Serial Number
  • Manufacturing Date

Other properties (12)

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