Identity
- Trade Name
- Bulb FDA UDI
- Generic Name
- Blood pressure cuff inflator, manual FDA UDI
- Device Name
- Bulb with Chrome-plated Air-valve FDA UDI
- Model / Reference
- BB00-0001 FDA UDI
- Description
- Bulb with Chrome-plated Air-valve FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00858293006489 FDA UDI
- FDA Product Code
- MON FDA UDI
- GMDN Term
- Blood pressure cuff inflator, manual 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Blood pressure cuff inflator, manual
Bulb by Reprocessing Products Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Medline — MEDLINE INDUSTRIES, INC. · Class II
- Medline — MEDLINE INDUSTRIES, 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 a2b98747-9dc6-43b9-8546-8b6b51da3b4b 33 fields · synced Jun 8, 2026