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Passing Needle Kit with Obturator

FDA UDI

Class I (US FDA UDI)

by Ad-Tech Medical Instrument Corp.

Identity

Trade Name
Passing Needle Kit with Obturator FDA UDI
Generic Name
Wire/ligature passer, reusable FDA UDI
Model / Reference
APNK1-3.5X FDA UDI

Identifiers

Catalog Number
APNK1-3.5X FDA UDI
Primary DI / UDI-DI
00841823100429 FDA UDI
FDA Product Code
HWQ FDA UDI
GMDN Term
Wire/ligature passer, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Wire/ligature passer, reusable

Passing Needle Kit with Obturator by Ad-Tech Medical Instrument Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire/ligature passer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 012de05e-e6ee-47ac-a7be-19b3aebac496 35 fields · synced Jun 9, 2026