Identity
- Trade Name
- EndoRotor® PED Purge Kit FDA UDI
- Generic Name
- Device lumen washing/disinfection attachment, single-use FDA UDI
- Device Name
- EndoRotor® PED Purge Kit FDA UDI
- Model / Reference
- PED-PURGE FDA UDI
- Description
- EndoRotor® PED Purge Kit FDA UDI
Identifiers
- Catalog Number
- PED-PURGE FDA UDI
- Primary DI / UDI-DI
- 00854172008230 FDA UDI
- FDA Product Code
- PTE FDA UDI
- GMDN Term
- Device lumen washing/disinfection attachment, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1690 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Device lumen washing/disinfection attachment, single-use
EndoRotor® PED Purge Kit by Interscope, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Device lumen washing/disinfection attachment, single-use.
- EndoRotor® Purge Kit (Single) — INTERSCOPE, INC · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Interscope, Inc
Sources (1)
- FDA UDI 07f679ac-c91d-4a13-b226-c1b19bec8c31 35 fields · synced Jun 6, 2026