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Arom-Cot

FDA UDI

Class I (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
AROM-COT FDA UDI
Generic Name
Amniotome, single-use FDA UDI
Device Name
AROM-COT FINGERCOT W/ATTACHED HOOK FDA UDI
Model / Reference
Small FDA UDI
Description
AROM-COT FINGERCOT W/ATTACHED HOOK FDA UDI

Identifiers

Catalog Number
AR100 FDA UDI
Primary DI / UDI-DI
H671AR1000 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

No

FDA UDI

Category: Amniotome, single-use

Arom-Cot by Utah Medical 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 8f7f76b2-9e13-4d85-981a-a6601f710b26 35 fields · synced Jun 9, 2026