Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Laryngeal knife FDA UDI
- Device Name
- JAKO CIRCLE KNIFE FDA UDI
- Model / Reference
- IPN007884 FDA UDI
- Description
- JAKO CIRCLE KNIFE FDA UDI
Identifiers
- Catalog Number
- 506665 FDA UDI
- Primary DI / UDI-DI
- 24026704531602 FDA UDI
- FDA Product Code
- KTG FDA UDI
- GMDN Term
- Laryngeal knife FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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
Dimensions & Sizes
- Size
- Length — 260 Millimeter FDA UDI
Category: Laryngeal knife
Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Laryngeal knife.
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- FENTEX — FENTEX medical GmbH · Class I
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- Integra® — Integra LifeSciences Production Corporation · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- JEDMED — JEDMED Instrument Company · Class I
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 f2d685b1-c27f-4c31-b5f8-2683f7a8cbb4 36 fields · synced May 30, 2026