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Pneupac 530A1167

by ICU Medical, Inc.

Pneupac 530A1167 is a Class II device made by ICU Medical, Inc., listed in FDA GUDID since 1 Sep 2015 (UDI-DI 35019315107478), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number35019315107478 UDI-DI Date1 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pneupac
Generic name
Transport electric ventilator
Model / reference
530A1167
Primary DI / UDI-DI
35019315107478
FDA product code
BTL
GMDN term
Transport electric ventilator
Device class
Class II
Regulation number
868.5925
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Transport electric ventilator

Similar devices in this category

Other devices filed under Transport electric ventilator.

Other devices from ICU Medical, Inc.

See all devices from ICU Medical, Inc. →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)