Identity
- Trade Name
- Os Finder FDA UDI
- Generic Name
- Fixed-diameter cervical dilator, single-use FDA UDI
- Device Name
- OS Finder Cervical dilators FDA UDI
- Model / Reference
- 1176 FDA UDI
- Description
- OS Finder Cervical dilators FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937017014 FDA UDI
- FDA Product Code
- HDQ FDA UDI
- GMDN Term
- Fixed-diameter cervical dilator, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.4530 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Fixed-diameter cervical dilator, single-use
Os Finder by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Fixed-diameter cervical dilator, single-use.
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- Centurion — Centurion Medical Products · Class II
- Bioseal Inc. — BIOSEAL · Class I
- Centurion — Centurion Medical Products · 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 |
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Manufacturer
- Manufacturer
- CooperSurgical, Inc.
Sources (1)
- FDA UDI 9bf620a5-52df-4281-bbc0-1563afbff00c 33 fields · synced Jun 9, 2026