Identity
- Trade Name
- Medline FDA UDI
- Generic Name
- Blood pressure cuff, single-use FDA UDI
- Device Name
- CUFF,BP,DISP,VINYL,1 TB,CHILD LNG,HP FDA UDI
- Model / Reference
- MDS9721HPLV FDA UDI
- Description
- CUFF,BP,DISP,VINYL,1 TB,CHILD LNG,HP FDA UDI
Identifiers
- Catalog Number
- MDS9721HPLV FDA UDI
- Primary DI / UDI-DI
- 10884389106211 FDA UDI
- FDA Product Code
- DXQ FDA UDI
- GMDN Term
- Blood pressure cuff, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1120 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
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: Blood pressure cuff, single-use
Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Blood pressure cuff, single-use.
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- Regard™ — RESOURCE OPTIMIZATION & INNOVATION, L.L.C. · Class II
- Orantech — Orantech Inc. · Class II
- Unimed — Unimed Medical Supplies, 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 II | Pending data |
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Manufacturer
- Manufacturer
- Medline Industries, Inc.
Sources (1)
- FDA UDI e9262a1e-8203-49f3-ac1f-82245be8099d 35 fields · synced Jun 8, 2026