Skip to content

PDO Max Cannulas CAN21100

by Max Pdo Inc

PDO Max Cannulas CAN21100 is a medical device (FDA Class I; FDA product code GEA, Cannula, Surgical, General & Plastic Surgery) made by Max Pdo Inc, listed in FDA GUDID since 24 Mar 2021 (UDI-DI 00850018324472), 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 Number00850018324472 UDI-DI Date24 Mar 2021ListedStatusListed 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  • Withdrawn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
PDO Max Cannulas
Generic name
Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use
Model / Ref / Catalog
CAN21100
Primary DI / UDI-DI
00850018324472
FDA product code
GEA
GMDN term
Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GEA (Cannula, Surgical, General & Plastic Surgery).

Other devices from Max Pdo Inc

See all devices from Max Pdo Inc →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)