Identity
- Trade Name
- DERMATOSCOPE / CAPILLAROSCOPE FDA UDI
- Generic Name
- Otoscope, direct FDA UDI
- Device Name
- DERMATOSCOPE / CAPILLAROSCOPE FDA UDI
- Model / Reference
- BTS-310 FDA UDI
- Description
- DERMATOSCOPE / CAPILLAROSCOPE FDA UDI
Identifiers
- Catalog Number
- FEDMEDMICFISTD_US FDA UDI
- Primary DI / UDI-DI
- B1623101 FDA UDI
- FDA Product Code
- ERA FDA UDI
- GMDN Term
- Otoscope, direct FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4770 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Dermatoscope / Capillaroscope by Bellegrove Medical Supply, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Bellegrove Medical Supply, Inc.
Sources (1)
- FDA UDI c725010f-eac8-4e5f-ba6f-6685a68cb50f 35 fields · synced Jun 1, 2026