E.m.adams, Inc.

FDA UDI

Class II (US FDA UDI)

by E.M. Adams

Identity

Trade Name: E.M.ADAMS, INC. FDA UDI
Generic Name: Circumcision kit, single-use FDA UDI
Model / Reference: 114 A7006 FDA UDI

Identifiers

Primary DI / UDI-DI: B121114A7006 FDA UDI
FDA Product Code: OHG FDA UDI
GMDN Term: Circumcision kit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.4530 FDA UDI
Commercial Distribution: Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

E.m.adams, Inc. by E.M. Adams — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 II	Pending data

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Manufacturer

Manufacturer: E.M. Adams

Sources (1)

FDA UDI ee5b7326-7f53-4e96-9702-e6c7aff44bda 33 fields · synced Jun 1, 2026