Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Ligature loop applier FDA UDI
- Device Name
- HOLLOW LUMEN PASSER PHEN HNDL 9 1/4" FDA UDI
- Model / Reference
- IPN020020 FDA UDI
- Description
- HOLLOW LUMEN PASSER PHEN HNDL 9 1/4" FDA UDI
Identifiers
- Catalog Number
- P23611 FDA UDI
- Primary DI / UDI-DI
- 14026704798893 FDA UDI
- FDA Product Code
- GDG FDA UDI
- GMDN Term
- Ligature loop applier 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: Ligature loop applier
Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 275a933c-74f2-499c-bf16-b1927a010f28 35 fields · synced Jun 8, 2026