Identity
- Trade Name
- Pumpmatic FDA UDI
- Generic Name
- User-induced pipette FDA UDI
- Device Name
- 1-101 FDA UDI
- Model / Reference
- 1-101 FDA UDI
- Description
- 1-101 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00689519021012 FDA UDI
- FDA Product Code
- GGY FDA UDI
- GMDN Term
- User-induced pipette FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.6160 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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 pipette
Pumpmatic by Ashton Pumpmatic, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as User-induced pipette.
- KOVA — KOVA INTERNATIONAL INC · Class I
- KOVA — KOVA INTERNATIONAL INC · Class I
- KOVA — KOVA INTERNATIONAL INC · Class I
- Transfer pipette 3.5ml — Sarstedt Aktiengesellschaft & Co.KG · Class I
- KOVA — KOVA INTERNATIONAL INC · Class I
- IVF Pasteur Pipets — CooperSurgical, Inc. · Class II
- Transfer pipette 3.5ml — Sarstedt Aktiengesellschaft & Co.KG · Class I
- Transfer pipette 3.5ml — Sarstedt Aktiengesellschaft & Co.KG · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ashton Pumpmatic, Inc.
Sources (1)
- FDA UDI 793bf60c-7320-42ce-ae3f-b1c29be70770 33 fields · synced May 31, 2026