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MedGyn Disposable Amnio Hook

FDA UDI

Class I (US FDA UDI)

by Medgyn Products, Inc.

Identity

Trade Name
MedGyn Disposable Amnio Hook FDA UDI
Generic Name
Amniotome, single-use FDA UDI
Device Name
MedGyn Disposable Amnio Hook FDA UDI
Model / Reference
Amniotome FDA UDI
Description
MedGyn Disposable Amnio Hook FDA UDI

Identifiers

Catalog Number
020301 FDA UDI
Primary DI / UDI-DI
M803020301 FDA UDI
FDA Product Code
HGE FDA UDI
GMDN Term
Amniotome, 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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Amniotome, single-use

MedGyn Disposable Amnio Hook by Medgyn Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Amniotome, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 79e010ea-28e4-4eb6-8d80-def739caf821 34 fields · synced May 30, 2026