Identity
- Trade Name
- EZ-Squeeze FDA UDI
- Generic Name
- Assisted reproduction microtool FDA UDI
- Device Name
- Assisted Reproduction Microtools (Pipettes) FDA UDI
- Model / Reference
- 135µm FDA UDI
- Description
- Assisted Reproduction Microtools (Pipettes) FDA UDI
Identifiers
- Catalog Number
- 7-72-3135/20 FDA UDI
- Primary DI / UDI-DI
- 05060488047244 FDA UDI
- 510(k) Number
- K161275 FDA UDI
- FDA Product Code
- MQH FDA UDI
- GMDN Term
- Assisted reproduction microtool FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.6130 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Assisted reproduction microtool
EZ-Squeeze by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Assisted reproduction microtool.
- ASTEC — ASTEC BIO USA INC · Class II
- ASTEC — ASTEC BIO USA INC · Class II
- EZ-Tip — Research Instruments , Ltd. · Class II
- RI Pipettes — Research Instruments , Ltd. · Class II
- ASTEC — ASTEC BIO USA INC · Class II
- STRIPPER — ORIGIO INC. · Class II
- RI Pipettes — Research Instruments , Ltd. · Class II
- STRIPPER — ORIGIO INC. · Class II
Cleared under the same submission
K161275 also covers:
- EZ-Squeeze — CooperSurgical, Inc.
- EZ-Squeeze — CooperSurgical, Inc.
- EZ-Strip — CooperSurgical, Inc.
- EZ-Strip — CooperSurgical, Inc.
- EZ-Strip — CooperSurgical, Inc.
- EZ-Tip — CooperSurgical, Inc.
- EZ-Tip — CooperSurgical, Inc.
- EZ-Tip — CooperSurgical, Inc.
- EZ-Tip — CooperSurgical, Inc.
- EZ-Tip — CooperSurgical, Inc.
- EZ-Tip — CooperSurgical, Inc.
- EZ-Tip — CooperSurgical, Inc.
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- CooperSurgical, Inc.
Sources (1)
- FDA UDI c7488f78-c685-49cb-80cf-ae1fea1776df 36 fields · synced Jun 9, 2026