Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Mastoid gauge FDA UDI
- Model / Reference
- IPN927647 FDA UDI
Identifiers
- Catalog Number
- P27789 FDA UDI
- Primary DI / UDI-DI
- 14026704912558 FDA UDI
- FDA Product Code
- KAK FDA UDI
- GMDN Term
- Mastoid gauge 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: Mastoid gauge
Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Mastoid gauge.
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- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Adler Instrument Company — Adler, Inc. · 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 048958ec-699f-4690-b8e6-cb8cc70bf0f8 34 fields · synced Jun 8, 2026