Identity
- Trade Name
- STERLING FDA UDI
- Generic Name
- Fibreoptic dental light FDA UDI
- Device Name
- STERLING Handpiece 1:5 Increasing Fiber-Optic ERL 95 1:5 FDA UDI
- Model / Reference
- 5259-507 FDA UDI
- Description
- STERLING Handpiece 1:5 Increasing Fiber-Optic ERL 95 1:5 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00366975013040 FDA UDI
- FDA Product Code
- EGS FDA UDI
- GMDN Term
- Fibreoptic dental light FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4200 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Fibreoptic dental light
Sterling by Benco Dental Supply Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Fibreoptic dental light.
- AdDent — Addent, Inc. · Class II
- AdDent — Addent, Inc. · Class II
- AIOBIO — AIOBIO Co., Ltd. · 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
- Benco Dental Supply Co.
Sources (1)
- FDA UDI 6274ffe9-9101-43f6-affa-be7d2b4d5427 34 fields · synced May 30, 2026