gudid
Primary ID: 88015
PeelPro (UDI 88015)
Manufactured by Sultan Healthcare Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PeelPro - Primary ID 88015
Device Regulatory Overview
The PeelPro (Model/Catalog Number: 88015) is a medical device manufactured by Sultan Healthcare Inc. This product is indexed under FDA Product Code / Category Classification KCT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 88015
- Product Code / EMDN
- KCT
- Device Name
- PeelPro Self-Sealing Sterilization Pouch 5.25 x 11 (133mm x 279mm) Box of 200
- Database Sync Date
- 2026-08-09 09:03:02
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of PeelPro?
The registered manufacturer of record for PeelPro is Sultan Healthcare Inc.
What is the Primary UDI-DI identifier for PeelPro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 88015.
What classification code is assigned to this device?
This device is registered under product classification code KCT.
Similar Classification Devices (KCT)
Other Devices by Sultan Healthcare Inc
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