← Back to catalogue

Aztec

FDA UDI

Class I (US FDA UDI)

by Aztecmed/Ent LLC

Identity

Trade Name
Aztec FDA UDI
Generic Name
Open-surgery biopsy forceps, reusable FDA UDI
Device Name
Blakesley Large Forcep 45 degree upturn FDA UDI
Model / Reference
10-15304 FDA UDI
Description
Blakesley Large Forcep 45 degree upturn FDA UDI

Identifiers

Catalog Number
10-15304 FDA UDI
Primary DI / UDI-DI
B87110153040 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
Open-surgery biopsy forceps, 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: Open-surgery biopsy forceps, reusable

Aztec by Aztecmed/Ent LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery biopsy forceps, reusable.

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
Aztecmed/Ent LLC

Sources (1)

  • FDA UDI 60f75a90-1bb4-4d6b-a44b-4e84c4b75293 34 fields · synced May 30, 2026