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Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Orthopaedic chisel blade FDA UDI
Device Name
PERIOTOME BLADE 2MM FOR MICRO COMPASS SAW FDA UDI
Model / Reference
3441681 FDA UDI
Description
PERIOTOME BLADE 2MM FOR MICRO COMPASS SAW FDA UDI

Identifiers

Catalog Number
3441681 FDA UDI
Primary DI / UDI-DI
00614950016938 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Orthopaedic chisel blade FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 2 Millimeter FDA UDI

Category: Orthopaedic chisel blade

Ace by Ace Surgical Supply Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic chisel blade.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b6f4ecb-eb76-443e-9eef-91bee97248df 37 fields · synced May 30, 2026