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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
Bone-angle protractor FDA UDI
Device Name
PROTRACTOR CEPHALOMETRIC L/F *COLD STERILIZE ONLY* FDA UDI
Model / Reference
0032936 FDA UDI
Description
PROTRACTOR CEPHALOMETRIC L/F *COLD STERILIZE ONLY* FDA UDI

Identifiers

Catalog Number
0032936 FDA UDI
Primary DI / UDI-DI
00614950025503 FDA UDI
FDA Product Code
HTH FDA UDI
GMDN Term
Bone-angle protractor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4600 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
High-level Disinfectant FDA UDI

Category: Bone-angle protractor

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

Similar devices

Also classified as Bone-angle protractor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ace Surgical Supply Co., Inc.

Sources (1)

  • FDA UDI cfa4288c-20c4-4c00-9dca-592132f369b0 36 fields · synced May 30, 2026