Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name: ACE FDA UDI
Generic Name: Hand-held dental retractor FDA UDI
Device Name: RETRACTOR LIP PLASTIC UNIVERSL ADULT/CHILD 2/PKG AUTOCLAVABLE L/F 4" 10CM FDA UDI
Model / Reference: 0100030 FDA UDI
Description: RETRACTOR LIP PLASTIC UNIVERSL ADULT/CHILD 2/PKG AUTOCLAVABLE L/F 4" 10CM FDA UDI

Identifiers

Catalog Number: 0100030 FDA UDI
Primary DI / UDI-DI: 00614950017089 FDA UDI
FDA Product Code: EIG FDA UDI
GMDN Term: Hand-held dental retractor FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 4 Inch FDA UDI

Category: Hand-held dental retractor

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

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EXPANDER — KLS-Martin L.P. · Class I
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BMT Medizintechnik GmbH — BMT Medizintechnik GmbH · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Ace Surgical Supply Co., Inc.

Sources (1)

FDA UDI 4b589a29-1211-4e52-88e6-eac076145779 37 fields · synced Jun 8, 2026