Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Ambulatory recorder conductive patch FDA UDI
- Device Name
- SUTURE PASSER HOLLOW LUMEN 7.25" FDA UDI
- Model / Reference
- IPN020019 FDA UDI
- Description
- SUTURE PASSER HOLLOW LUMEN 7.25" FDA UDI
Identifiers
- Catalog Number
- P23610 FDA UDI
- Primary DI / UDI-DI
- 14026704798886 FDA UDI
- FDA Product Code
- GDG FDA UDI
- GMDN Term
- Ambulatory recorder conductive patch 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
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Ambulatory recorder conductive patch
Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Ambulatory recorder conductive patch.
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- EKG Patch (Pediatric 3) — MG MEDICAL PRODUCTS LLC · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 227b5116-f6b0-485f-8d6f-8603d44f993e 35 fields · synced May 30, 2026