Identity
- Trade Name
- D-Vapor 3000 FDA UDI
- Generic Name
- Desflurane anaesthesia vaporizer FDA UDI
- Model / Reference
- M36700 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04048675301370 FDA UDI
- 510(k) Number
- K042276 FDA UDI
- FDA Product Code
- CAD FDA UDI
- GMDN Term
- Desflurane anaesthesia vaporizer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5880 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Desflurane anaesthesia vaporizer
D-Vapor 3000 by Drägerwerk AG & Co. KGaA — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Desflurane anaesthesia vaporizer.
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Cleared under the same submission
K042276 also covers:
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Drägerwerk AG & Co. KGaA
Sources (2)
- FDA UDI 4d865089-620c-45a5-8d5f-5ff02d26fb6c 34 fields · synced Jun 19, 2026
- EUDAMED 1 fields · synced Jun 19, 2026