Identity
- Trade Name
- Symmetry Hegar FDA UDI
- Generic Name
- Urethral dilator, reusable FDA UDI
- Device Name
- Symmetry® Dilator, Hegar, Single-Ended, 3.5 mm Tip FDA UDI
- Model / Reference
- 52-3103 FDA UDI
- Description
- Symmetry® Dilator, Hegar, Single-Ended, 3.5 mm Tip FDA UDI
Identifiers
- Catalog Number
- 52-3103 FDA UDI
- Primary DI / UDI-DI
- 00887482172933 FDA UDI
- FDA Product Code
- HDQ FDA UDI
- GMDN Term
- Urethral dilator, reusable 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
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Width — 3.5 Millimeter FDA UDI
Category: Urethral dilator, reusable
Symmetry Hegar by Symmetry Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Urethral dilator, reusable.
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Symmetry Surgical Inc.
Sources (1)
- FDA UDI 7a6b4f60-3060-45d5-9509-c6c8a92a779d 36 fields · synced May 30, 2026