Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Rigid intubation laryngoscope, reusable FDA UDI
- Device Name
- GARRETT-OSSOFF-PILLING LARYNG 25MM X 19CM FDA UDI
- Model / Reference
- IPN002711 FDA UDI
- Description
- GARRETT-OSSOFF-PILLING LARYNG 25MM X 19CM FDA UDI
Identifiers
- Catalog Number
- 522196 FDA UDI
- Primary DI / UDI-DI
- 04026704714605 FDA UDI
- FDA Product Code
- CCW FDA UDI
- GMDN Term
- Rigid intubation laryngoscope, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5540 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: Rigid intubation laryngoscope, reusable
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 4dc390b3-7d43-4ff2-b1e0-be041aa4052c 35 fields · synced Jun 8, 2026