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PDO Max Cannulas

FDA UDI

Class I (US FDA UDI)

by Max Pdo Inc

Identity

Trade Name
PDO Max Cannulas FDA UDI
Generic Name
Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use FDA UDI
Device Name
Cannula 22gx70mm. Cannula, Surgical, General and Plastic Surgery FDA UDI
Model / Reference
YC-22-70 (UTW) FDA UDI
Description
Cannula 22gx70mm. Cannula, Surgical, General and Plastic Surgery FDA UDI

Identifiers

Catalog Number
YC-22-70 (UTW) FDA UDI
Primary DI / UDI-DI
00850018324700 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use

PDO Max Cannulas by Max Pdo Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Max Pdo Inc

Sources (1)

  • FDA UDI d7668ede-7759-482b-9c28-1c360be75e18 34 fields · synced Jun 1, 2026