← Back to catalogue

NGHS Tubal RFID

FDA UDI

by Packroom Llc

Identity

Trade Name
NGHS Tubal RFID FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
NGHS Tubal RFID FDA UDI
Model / Reference
NG120RFPBC FDA UDI
Description
NGHS Tubal RFID FDA UDI

Identifiers

Primary DI / UDI-DI
00817395023848 FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

NGHS Tubal RFID by Packroom Llc — 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

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

Manufacturer

Manufacturer
Packroom Llc

Sources (1)

  • FDA UDI a23d010b-9c2e-4d74-90b8-b4a06d021354 33 fields · synced Jun 8, 2026