Identity
- Trade Name
- Novo Surgical FDA UDI
- Generic Name
- Wire-extracting pliers FDA UDI
- Device Name
- zenith wire pulling forceps, max capacity 1.0 mm, 6-1/2" (16.5 cm) FDA UDI
- Model / Reference
- N92567-47 FDA UDI
- Description
- zenith wire pulling forceps, max capacity 1.0 mm, 6-1/2" (16.5 cm) FDA UDI
Identifiers
- Catalog Number
- N92567-47 FDA UDI
- Primary DI / UDI-DI
- G586N92567470 FDA UDI
- FDA Product Code
- HTC FDA UDI
- GMDN Term
- Wire-extracting pliers 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Wire-extracting pliers
Novo Surgical by Novo Surgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wire-extracting pliers.
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- WIRE EXTRACTION PLIERS — SONTEC INSTRUMENTS, INC. · Class I
- PIN PULLER — SONTEC INSTRUMENTS, INC. · Class I
- gSource — GSOURCE, LLC. · Class I
- AESCULAP — AESCULAP, 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
- Novo Surgical, Inc.
Sources (1)
- FDA UDI ecd89ca1-9e5c-4f83-b91d-8742a1c4daaa 35 fields · synced May 30, 2026