Identity
- Trade Name
- BV Medical FDA UDI
- Generic Name
- Percussion hammer, manual, reusable FDA UDI
- Device Name
- Combo Kit: Orange EMT Fanny Pack: 38-416-194 Sprague Rappaport-Type, Adult, Orange, Latex Free, 20-218-194-L Classic Aneroid Sphygmomanometer, Orange Nylon Cuff, Adult, Latex Free PVC: 60-125-000 Penlight, High Intensity, Reusable, White: 8-380J Fiberglass Tape Measure, BV Logo Sticker, White Case: 80-500-999 Taylor Percussion Hammer, Stealth: 80-170-010 Utility scissors 5.5", stainless steel with black handle FDA UDI
- Model / Reference
- 20-443-194-L FDA UDI
- Description
- Combo Kit: Orange EMT Fanny Pack: 38-416-194 Sprague Rappaport-Type, Adult, Orange, Latex Free, 20-218-194-L Classic Aneroid Sphygmomanometer, Orange Nylon Cuff, Adult, Latex Free PVC: 60-125-000 Penlight, High Intensity, Reusable, White: 8-380J Fiberglass Tape Measure, BV Logo Sticker, White Case: 80-500-999 Taylor Percussion Hammer, Stealth: 80-170-010 Utility scissors 5.5", stainless steel with black handle FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00845821026156 FDA UDI
- FDA Product Code
- GWZ FDA UDIFTY FDA UDILRW FDA UDIKYT FDA UDILDE FDA UDIDXQ FDA UDI
- GMDN Term
- Percussion hammer, manual, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.1700 FDA UDI878.4800 FDA UDI880.6350 FDA UDI870.1875 FDA UDI870.1120 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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose surgical scissors, reusableAneroid manual sphygmomanometerMechanical external stethoscopePercussion hammer, manual, reusable
BV Medical by Medical, Inc. — 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
- Medical, Inc.
Sources (1)
- FDA UDI f8dbfc60-d886-4fa9-9398-633b7fd40094 34 fields · synced May 30, 2026