Identity
- Trade Name
- Integra® Miltex® FDA UDI
- Generic Name
- Tracheal bistoury FDA UDI
- Device Name
- Integra® Miltex® Jackson Tracheal Bistoury 7", Curved Blade FDA UDI
- Model / Reference
- 23-1060 FDA UDI
- Description
- Integra® Miltex® Jackson Tracheal Bistoury 7", Curved Blade FDA UDI
Identifiers
- Catalog Number
- 23-1060 FDA UDI
- Primary DI / UDI-DI
- 10381780424932 FDA UDI
- FDA Product Code
- KCC FDA UDI
- GMDN Term
- Tracheal bistoury 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Tracheal bistoury
Integra® Miltex® by Integra LifeSciences Production Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tracheal bistoury.
- gSource — GSOURCE, LLC. · Class I
- Integra® Jarit® — Integra LifeSciences Production Corporation · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI 78b445b0-4c74-45e5-b6a3-9e2fd7cdabe6 35 fields · synced Jun 9, 2026