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NovaSure

FDA UDI

Class III (US FDA UDI)

by Hologic, Inc.

Identity

Trade Name
NovaSure FDA UDI
Generic Name
Radio-frequency endometrial-ablation system handpiece/electrode FDA UDI
Device Name
The NovaSure® Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in pre-menopausal women with menorrhagia (excessive bleeding) due to benign causes for whom childbearing is complete. FDA UDI
Model / Reference
V5 FDA UDI
Description
The NovaSure® Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in pre-menopausal women with menorrhagia (excessive bleeding) due to benign causes for whom childbearing is complete. FDA UDI

Identifiers

Catalog Number
NSV5US-001 FDA UDI
Primary DI / UDI-DI
15420045514294 FDA UDI
PMA Number
P010013 FDA UDI
FDA Product Code
MNB FDA UDI
GMDN Term
Radio-frequency endometrial-ablation system handpiece/electrode FDA UDI

Classification

Device Class
Class III 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: Radio-frequency endometrial-ablation system handpiece/electrode

NovaSure by Hologic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radio-frequency endometrial-ablation system handpiece/electrode.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hologic, Inc.

Sources (1)

  • FDA UDI 72a63589-a6bf-410e-8980-cc7164c45ab6 36 fields · synced May 31, 2026