Identity
- Trade Name
- Guage FDA UDI
- Generic Name
- Aneroid manual sphygmomanometer FDA UDI
- Device Name
- Gauge, 0-300 mm Hg, 3/16 in. Hose Barb FDA UDI
- Model / Reference
- BG00-0300 FDA UDI
- Description
- Gauge, 0-300 mm Hg, 3/16 in. Hose Barb FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00858293006472 FDA UDI
- FDA Product Code
- MON FDA UDI
- GMDN Term
- Aneroid manual sphygmomanometer FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5820 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
Category: Aneroid manual sphygmomanometer
Guage by Reprocessing Products Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Aneroid manual sphygmomanometer.
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- Diagnostix™ — American Diagnostic Corporation · Class II
- E-sphyg™ — American Diagnostic Corporation · Class II
- BAUM — W.A. BAUM CO., INC. · Class II
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
- Reprocessing Products Corp
Sources (1)
- FDA UDI 2d4e5a29-23d2-41ea-913a-bb7a93075d8d 33 fields · synced May 30, 2026