Identity
- Trade Name
- Marketlab FDA UDI
- Generic Name
- User-induced micropipette FDA UDI
- Device Name
- Disposable Transfer Pipette, 3.0 mL FDA UDI
- Model / Reference
- 108154 FDA UDI
- Description
- Disposable Transfer Pipette, 3.0 mL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817517026214 FDA UDI
- FDA Product Code
- LXG FDA UDI
- GMDN Term
- User-induced micropipette 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
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
Yes
FDA UDI
Category: User-induced micropipette
Marketlab by Marketlab Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as User-induced micropipette.
- ICSI Pipette — Vitrolife Sweden AB · Class II
- SFG Holding pipettes — SPECTRUM FERTILITY GROUP INC. · Class II
- SFG Denuding pipettes — SPECTRUM FERTILITY GROUP INC. · Class II
- Hatching Pipette — Vitrolife Sweden AB · Class II
- ICSI Pipette — Vitrolife AB · Class II
- Biopsy Pipette — Vitrolife Sweden AB · Class II
- ICSI Pipette — Vitrolife AB · Class II
- Hatching Pipette — Vitrolife AB · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Marketlab Inc.
Sources (1)
- FDA UDI b96a98ed-a333-4b83-9ae6-cd73ee8b2c61 33 fields · synced Jun 8, 2026