GUDIDData
eudamed_udi Primary ID: 10888277417175

Sensicare PI Green (UDI 10888277417175)

Manufactured by Medline Industries, LP

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sensicare PI Green - Primary ID 10888277417175

Device Regulatory Overview

The Sensicare PI Green (Model/Catalog Number: MSG9280) is a medical device manufactured by Medline Industries, LP. This product is indexed under FDA Product Code / Category Classification T01010203 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2788-2026 View Full Alert →

Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART MOSES, Medline Kit SKU DYNJ910103B; 2) BASIC HEART CDS, Medlin...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-2789-2026 View Full Alert →

Medline medical convenience kits labeled as: 1) SHOULDER PACK, Medline Kit SKU DYNJ39590O; 2) SHOULDER PACK, Medline Kit SKU DYNJ88566;...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-2784-2026 View Full Alert →

Medline convenience kits containing Bard Silastic Foley Catheters (French sizes 16, 18, 20) 5cc balloons. ROBOTIC CDS980523M...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
MSG9280
Product Code / EMDN
T01010203
Device Name
Sensicare PI Green
Database Sync Date
2026-08-09 16:29:56

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Sensicare PI Green?

The registered manufacturer of record for Sensicare PI Green is Medline Industries, LP.

What is the Primary UDI-DI identifier for Sensicare PI Green?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10888277417175.

What classification code is assigned to this device?

This device is registered under product classification code T01010203.

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