Identity
- Trade Name
- BEAR FDA UDI
- Generic Name
- Craniofacial rongeur, reusable FDA UDI
- Device Name
- Takahashi Nasal Forceps, 3.0mm, 45 Degree FDA UDI
- Model / Reference
- 7.06.53 FDA UDI
- Description
- Takahashi Nasal Forceps, 3.0mm, 45 Degree FDA UDI
Identifiers
- Catalog Number
- 7.06.53 FDA UDI
- Primary DI / UDI-DI
- G043706530 FDA UDI
- FDA Product Code
- KAX FDA UDI
- GMDN Term
- Craniofacial rongeur, reusable 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: Craniofacial rongeur, reusable
Bear by Bear-Ent, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Wiggins Medical — EBNER MEDICAL LLC · 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
- Bear-Ent, LLC
Sources (1)
- FDA UDI caa2b287-6df8-4495-b300-043a8cdc9fd1 34 fields · synced May 31, 2026