Identity
- Trade Name
- SURJEX FDA UDI
- Generic Name
- Hand-held surgical retractor, reusable FDA UDI
- Device Name
- CLOWARD BLADE RETRACTOR 7.5" BLADE 13MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 18MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 20MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 23MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 30MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 33MM WITH LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 13MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 18MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 20MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 23MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 30MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 33MM NO LIP FDA UDI
- Model / Reference
- WM9873320 to WM9873333 FDA UDI
- Description
- CLOWARD BLADE RETRACTOR 7.5" BLADE 13MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 18MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 20MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 23MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 30MM WITH LIP CLOWARD BLADE RETRACTOR 7.5" BLADE 33MM WITH LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 13MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 18MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 20MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 23MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 30MM NO LIP CLOWARD MODI CERVICAL RETRACTOR BLADE 7.5" 33MM NO LIP FDA UDI
Identifiers
- Catalog Number
- WM9873320 to WM9873333 FDA UDI
- Primary DI / UDI-DI
- G383CLOWARDBLADERETRAF6 FDA UDI
- FDA Product Code
- GAD FDA UDI
- GMDN Term
- Hand-held surgical retractor, 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
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Category: Hand-held surgical retractor, reusable
Surjex by Surjex — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hand-held surgical retractor, reusable.
- ATLAS — ATLAS CERRAHİ ALETLER LTD. ŞTİ. · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- MİKRO — SAMSUN MİKRO CERRAHİ ALETLER İMALAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ · Class I
- Gimmi — Gimmi GmbH · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Sklar® — Sklar Corporation · Class I
- BIOCOMPOSITE PLUS ANCHOR Ø3, 5 MM W/NEEDLE — BMT BAPS BİYO MALZEME SANAYİ VE TİCARET ANONİM ŞİRKETİ · Class III
- Spreizer / Spreader — REDA Instrumente 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Surjex
Sources (1)
- FDA UDI a9a8932f-d64e-4fce-9c1a-632bd06d0e43 35 fields · synced May 30, 2026