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Aztec

FDA UDI

Class I (US FDA UDI)

by Aztecmed/Ent LLC

Identity

Trade Name
Aztec FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
Sinus Cup Forcep 3mm FDA UDI
Model / Reference
10-16203 FDA UDI
Description
Sinus Cup Forcep 3mm FDA UDI

Identifiers

Catalog Number
10-16203 FDA UDI
Primary DI / UDI-DI
B87110162030 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Discover the Sinus Cup Forcep 3mm, a versatile and effective surgical soft-tissue manipulation instrument designed for precise grasping and manipulation in ENT procedures. This reusable forceps are engineered with high-grade stainless steel, available in various sizes, and can be sterilized prior to use.

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, tweezers-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aztecmed/Ent LLC

Sources (1)

  • FDA UDI 632d0547-10c1-41a3-8119-cd0e088fbeda 34 fields · synced Jul 26, 2026