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McMahan Cervico Meter

FDA UDI

Class I (US FDA UDI)

by Medgyn Products, Inc.

Identity

Trade Name
McMahan Cervico Meter FDA UDI
Generic Name
Fixed-diameter cervical dilator, reusable FDA UDI
Device Name
McMahan Cervico Meter FDA UDI
Model / Reference
McMahan Cervico Meter FDA UDI
Description
McMahan Cervico Meter FDA UDI

Identifiers

Catalog Number
031300 FDA UDI
Primary DI / UDI-DI
M803031300 FDA UDI
FDA Product Code
HDQ FDA UDI
GMDN Term
Fixed-diameter cervical 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Fixed-diameter cervical dilator, reusable

McMahan Cervico Meter by Medgyn Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixed-diameter cervical dilator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0b2438cc-1aa0-49d5-a290-15a443eaa6db 34 fields · synced Jun 8, 2026