← Back to catalogue

NIPS Single Pack Testing Kit

FDA UDI

Class I (US FDA UDI)

by Ditek Consulting Llc

Identity

Trade Name
NIPS Single Pack Testing Kit FDA UDI
Generic Name
Phlebotomy kit FDA UDI
Device Name
NIPS Single Pack Testing Kit FDA UDI
Model / Reference
116373 FDA UDI
Description
NIPS Single Pack Testing Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00860011770220 FDA UDI
FDA Product Code
OIB FDA UDI
GMDN Term
Phlebotomy kit 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: Phlebotomy kit

NIPS Single Pack Testing Kit by Ditek Consulting Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phlebotomy kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 7ec3b6b5-ea6e-40cf-811e-7f6e823b5791 33 fields · synced Jun 8, 2026