← Back to catalogue

Safe-T-Surg

FDA UDI

Class I (US FDA UDI)

by BihlerMed, L.L.C.

Identity

Trade Name
Safe-T-Surg FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Safe-T-Surg Retractor FDA UDI
Model / Reference
2804-01-0001 FDA UDI
Description
Safe-T-Surg Retractor FDA UDI

Identifiers

Primary DI / UDI-DI
10865082000167 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical retractor/retraction system blade, reusable

Safe-T-Surg by BihlerMed, L.L.C. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
BihlerMed, L.L.C.

Sources (1)

  • FDA UDI 1c9bf2c7-dd44-49a6-8631-f692307ac231 34 fields · synced Jun 8, 2026