Identity
- Trade Name
- Multi Sealer MS 1000 FDA UDI
- Generic Name
- Blood donor bag tube divider/sealer FDA UDI
- Model / Reference
- 87.7708.800 FDA UDI
Identifiers
- Catalog Number
- 87.7708.800 FDA UDI
- Primary DI / UDI-DI
- 04038917341608 FDA UDI
- FDA Product Code
- KSD FDA UDI
- GMDN Term
- Blood donor bag tube divider/sealer FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.9750 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Blood donor bag tube divider/sealer
Multi Sealer MS 1000 by Sarstedt Aktiengesellschaft & Co.KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Sarstedt Aktiengesellschaft & Co.KG
Sources (1)
- FDA UDI 12149abb-f91e-4641-81bc-3b5062efc6b6 34 fields · synced May 30, 2026