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Bishop Retractor

FDA UDI

Class I (US FDA UDI)

by Salvin Dental Specialties, Llc

Identity

Trade Name
Bishop Retractor FDA UDI
Generic Name
Dental cheek retractor, professional, reusable FDA UDI
Model / Reference
BISHOP-RETRACT FDA UDI

Identifiers

Primary DI / UDI-DI
00841336103870 FDA UDI
FDA Product Code
KBL FDA UDI
GMDN Term
Dental cheek retractor, professional, 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

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
Moist Heat or Steam Sterilization FDA UDI

Category: Dental cheek retractor, professional, reusable

Bishop Retractor by Salvin Dental Specialties, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental cheek retractor, professional, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d68a3bdd-5302-4037-95b5-9647063f075c 32 fields · synced Jun 1, 2026