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Ventlab VN2100MCP

by Ventlab Corp.

Ventlab VN2100MCP is a Class II device made by Ventlab Corp., listed in FDA GUDID since 6 Dec 2016 (UDI-DI 10889483094525), 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 Number10889483094525 UDI-DI Date6 Dec 2016ListedStatusListed 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  • Withdrawn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
Ventlab
Generic name
Pulmonary resuscitator, manual, single-use
Model / reference
VN2100MCP
Primary DI / UDI-DI
10889483094525
FDA product code
BTM
GMDN term
Pulmonary resuscitator, manual, single-use
Device class
Class II
Regulation number
868.5915
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 1000 Milliliter

Related devices

Category: Pulmonary resuscitator, manual, single-use

Similar devices in this category

Other devices filed under Pulmonary resuscitator, manual, single-use.

Other devices from Ventlab Corp.

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Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)