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NMS Umbilical Cord Kit

FDA UDI

Class I (US FDA UDI)

by Ditek Consulting Llc

Identity

Trade Name
NMS Umbilical Cord Kit FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
NMS Umbilical Cord Kit FDA UDI
Model / Reference
380371G FDA UDI
Description
NMS Umbilical Cord Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00860013969530 FDA UDI
FDA Product Code
OIB FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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: General surgical procedure kit, non-medicated, single-use

NMS Umbilical Cord Kit by Ditek Consulting Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ditek Consulting Llc

Sources (1)

  • FDA UDI bd9028b5-7275-46c7-aa0b-9c2af03a64a0 33 fields · synced May 30, 2026