← Back to catalogue

18G Wallace Single Lumen Oocyte Recovery Set

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
18G Wallace Single Lumen Oocyte Recovery Set FDA UDI
Generic Name
IVF oocyte aspiration needle, single-use FDA UDI
Device Name
18G Wallace Single Lumen Oocyte Recovery Set, 950 mm tubing (Box of 10) FDA UDI
Model / Reference
ONS1833 FDA UDI
Description
18G Wallace Single Lumen Oocyte Recovery Set, 950 mm tubing (Box of 10) FDA UDI

Identifiers

Primary DI / UDI-DI
00888937021103 FDA UDI
FDA Product Code
MQE FDA UDI
GMDN Term
IVF oocyte aspiration needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6100 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
Length — 950 Millimeter FDA UDI
Needle Gauge — 18 Gauge FDA UDI

Category: IVF oocyte aspiration needle, single-use

18G Wallace Single Lumen Oocyte Recovery Set by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as IVF oocyte aspiration needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 675c383c-7c11-4829-af7c-a625ac1374f6 34 fields · synced Jun 9, 2026