Identity
- Trade Name
- Pipette tip FDA UDI
- Generic Name
- User-induced pipette FDA UDI
- Model / Reference
- 70.3070.210 FDA UDI
Identifiers
- Catalog Number
- 70.3070.210 FDA UDI
- Primary DI / UDI-DI
- 04066916032036 FDA UDI
- FDA Product Code
- JRC FDA UDI
- GMDN Term
- User-induced pipette FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2050 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: User-induced pipette
Pipette tip by Sarstedt Aktiengesellschaft & Co.KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as User-induced pipette.
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- Pumpmatic — ASHTON PUMPMATIC, INC. · Class I
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 5453b42f-afbc-41d9-bd13-167f1d5088b5 33 fields · synced Jun 8, 2026