Pilling IPN008752
by Teleflex Incorporated 2 variants
Pilling IPN008752 (526351) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 11 Aug 2022 (UDI-DI 14026704721617), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number14026704721617 | Date11 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 14026704721617
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pilling
- Generic name
- Laryngoscope handle, reusable
- Model / Ref / Catalog
- IPN008752, 526351
- Primary DI / UDI-DI
- 14026704721617
- FDA product code
- EQH
- GMDN term
- Laryngoscope handle, reusable
- Device class
- Class I
- Regulation number
- 874.4350
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 5.7 InchWidth — 5.5 Inch
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