Identity
- Trade Name
- J & J INSTRUMENTS FDA UDI
- Generic Name
- Hand-held dental retractor FDA UDI
- Device Name
- BALFOUR RETRACTOR 3.5"" SPREAD FDA UDI
- Model / Reference
- 41-1060 FDA UDI
- Description
- BALFOUR RETRACTOR 3.5"" SPREAD FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817524027686 FDA UDI
- FDA Product Code
- EIG FDA UDI
- GMDN Term
- Hand-held dental retractor FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 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
No
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
No
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: Hand-held dental retractor
J & J Instruments by J&J Instruments, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- J&J Instruments, LLC
Sources (1)
- FDA UDI dac2dccd-0599-4b86-a918-9d1c0495e032 33 fields · synced Jun 9, 2026