Identity
- Trade Name
- BOEHRINGER® CareDry™ Wand FDA UDI
- Generic Name
- Vacuum suction regulator/regulation set, general-purpose FDA UDI
- Device Name
- CareDry™ Wand FDA UDI
- Model / Reference
- 7640 FDA UDI
- Description
- CareDry™ Wand FDA UDI
Identifiers
- Catalog Number
- 7640 FDA UDI
- Primary DI / UDI-DI
- 10816286021038 FDA UDI
- FDA Product Code
- KDP FDA UDI
- GMDN Term
- Vacuum suction regulator/regulation set, general-purpose FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
BOEHRINGER® CareDry™ Wand by Boehringer Laboratories, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Boehringer Laboratories, Llc
Sources (1)
- FDA UDI a3570832-5574-4777-92b1-4d79e32d2d57 36 fields · synced May 30, 2026