Identity
- Trade Name
- CUFF FDA UDI
- Generic Name
- Blood pressure cuff, reusable FDA UDI
- Model / Reference
- 0683-15-0004-01 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06944904059556 FDA UDI
- GMDN Term
- Blood pressure cuff, reusable FDA UDI
Classification
- 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
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
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Blood pressure cuff, reusable
Cuff by Shenzhen Mindray Bio-Medical Electronics Co. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Disposable Cuff — SUNTECH MEDICAL, INC. · Class II
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- Welch Allyn, Inc. — Welch Allyn, 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Shenzhen Mindray Bio-Medical Electronics Co.
Sources (1)
- FDA UDI 3619209a-3080-47a0-8722-388679501676 32 fields · synced May 30, 2026