Identity
- Trade Name
- Wallace Embryo Replacement Catheter FDA UDI
- Generic Name
- Assisted reproduction transfer catheter/set FDA UDI
- Device Name
- Wallace Embryo Replacement Catheter, Intermediate 18 cm (Box of 10) FDA UDI
- Model / Reference
- 1816S FDA UDI
- Description
- Wallace Embryo Replacement Catheter, Intermediate 18 cm (Box of 10) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937021219 FDA UDI
- FDA Product Code
- MQF FDA UDI
- GMDN Term
- Assisted reproduction transfer catheter/set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.6110 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
Dimensions & Sizes
- Size
- Catheter Length — 18 Centimeter FDA UDI
Category: Assisted reproduction transfer catheter/set
Wallace Embryo Replacement Catheter by CooperSurgical, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- CooperSurgical, Inc.
Sources (1)
- FDA UDI ffc42e3d-b9a5-4c0c-bf5b-1ee1c9ae72bd 34 fields · synced Jun 9, 2026