ACE

Speculum Vienna Nasal Medium 5-1/2" 14CM

Registry build 21.09.26
1manufacturer
3catalogue numbers in this listing

Who Else Makes It

Registered in Shandong.

Chinese manufacturers registered for FDA product code KAG
Manufacturer City Province Registered as Device types
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222

Record

Regulatory record for ACE
Listed by Ace Surgical Supply Co., Inc., United States
FDA product code KAG
Device type Holder, Speculum, Ent
Device class Class 1
Regulation 21 CFR 878.1800
Premarket notification Exempt
Record published 2019-10-24

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Storage Special storage condition: No special storage conditions required
Sizes Length 5.5 in
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for ACE
Catalogue number Size Status
0618127 Length 5.5 in In distribution
0616125 Length 5.5 in In distribution
0617126 Length 5.5 in In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Lazic Peter Lazic Gmbh 18
Aesculap Aesculap AG 1

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer