Mixing wire 95.936
by Sarstedt Aktiengesellschaft & Co.KG
Ref 95.936
Active
CE IVDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDR EUDAMED | Number4038917SARTD03102U65 | Date13 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04038917234610 | Date11 Aug 2026 | StatusListed |
Certificates
No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Mischstäbchen EUDAMEDMixing wire GUDID
- Generic Name
- Capillary blood collection tube IVD, electrolyte-balanced heparin
- Model / Ref / Catalog
- 95.936
- Primary DI / UDI-DI
- 04038917234610
- Basic UDI-DI
- 4038917SARTD03102U65
- Unit of Use DI
- 04038917234627
- FDA Product Code
- GIO
- EMDN Code
- W0501010203 Blood collection, capillary tubes
- GMDN Term
- Capillary blood collection tube IVD, electrolyte-balanced heparin
- Device Class
- Class A EUDAMEDClass I GUDID
- Regulation Number
- 864.6150
- Market of Registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class A | Class I |
Other devices from Sarstedt Aktiengesellschaft & Co.KG
Properties
Other properties (20)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Human Tissues: No
- Animal Tissues: No
- Microbial Substances: No
- Reagent: No
- Self Testing: No
- Near-Patient Testing: No
- Professional Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No
- New Device: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No